Dear A06 Program Participants
Please finde reregistration form for BII Industry programs
For
BII
Friday, November 30, 2007
Reregistration Letter Industry Program in IPR
Bioinformatics Institute of India
C-56A/28, Sector-62, Noida - 201301, U.P. India, Tel.: 120-4320801/802
Industry program in Intellectual Property Rights
Distance Participation
Autumn 2006 Batch
Subject: Re-Registration due to non appearance /non-clearance of November 2007 exam
Dear Program Participant,
You have not been able to complete the program due to non-appearance / non clearance of all the papers in November 2007 exam. You can however still complete the programs by re-registering in the next session.
For the same you have to:
1. Submit Re-Registration form and Re-Registration fees Re-registration fees is Rs 5000/- USD 350 only. Re-Registration extends your registration for April 2008 and Nov 2008 examinations. The fees should be paid in the form of demand draft drawn in favour of “Bioinformatics Institute of India” payable at Delhi/New Delhi.
2. Submit exam form and exam fee for the exam in which you wish to appear. Exam fees is Rs 200/- / USD 25 per paper. So if you are to appear in four papers exam fees will be Rs 800/- / USD 100 only.
3. Submit Compulsory assignment & Research study (only in the case of non submission of the same earlier). You have to submit the same before April 2008 exam in which you wish to appear.
Please note:-
1. In order to complete Industry program in Intellectual Property Rights the participant will have to clear all the four papers along with the submission of Compulsory assignments and Research Study.
2. To continue in the program, re-registration within notified period is mandatory. If you do not re-register by 28th Feb 2008 , you will not be allowed to continue the program.
3. Participants can submit single Demand draft for re-registration fees and exam fees.
Important Dates:
Last date for re-registration to continue the program
28th February 2008
Last date for Examination form & fee submission for April 2008 exams
28th February 2008
Examination notification for April 2008 exams will be sent in the month of Feb 2008.
With best wishes,
Program Coordinator
Bioinformatics Institute of India
Enclosure: Re-registration form
BII BLOG: Join the Institute Blog at http://www.biinoida.blogspot.com/ for latest news, lectures, jobs and videos in the field of Bioinformatics, Clinical Trial, Pharma Regulatory Affairs, IPR, Pharma GMP etc.
C-56A/28, Sector-62, Noida - 201301, U.P. India, Tel.: 120-4320801/802
Industry program in Intellectual Property Rights
Distance Participation
Autumn 2006 Batch
Subject: Re-Registration due to non appearance /non-clearance of November 2007 exam
Dear Program Participant,
You have not been able to complete the program due to non-appearance / non clearance of all the papers in November 2007 exam. You can however still complete the programs by re-registering in the next session.
For the same you have to:
1. Submit Re-Registration form and Re-Registration fees Re-registration fees is Rs 5000/- USD 350 only. Re-Registration extends your registration for April 2008 and Nov 2008 examinations. The fees should be paid in the form of demand draft drawn in favour of “Bioinformatics Institute of India” payable at Delhi/New Delhi.
2. Submit exam form and exam fee for the exam in which you wish to appear. Exam fees is Rs 200/- / USD 25 per paper. So if you are to appear in four papers exam fees will be Rs 800/- / USD 100 only.
3. Submit Compulsory assignment & Research study (only in the case of non submission of the same earlier). You have to submit the same before April 2008 exam in which you wish to appear.
Please note:-
1. In order to complete Industry program in Intellectual Property Rights the participant will have to clear all the four papers along with the submission of Compulsory assignments and Research Study.
2. To continue in the program, re-registration within notified period is mandatory. If you do not re-register by 28th Feb 2008 , you will not be allowed to continue the program.
3. Participants can submit single Demand draft for re-registration fees and exam fees.
Important Dates:
Last date for re-registration to continue the program
28th February 2008
Last date for Examination form & fee submission for April 2008 exams
28th February 2008
Examination notification for April 2008 exams will be sent in the month of Feb 2008.
With best wishes,
Program Coordinator
Bioinformatics Institute of India
Enclosure: Re-registration form
BII BLOG: Join the Institute Blog at http://www.biinoida.blogspot.com/ for latest news, lectures, jobs and videos in the field of Bioinformatics, Clinical Trial, Pharma Regulatory Affairs, IPR, Pharma GMP etc.
Reregistration Letter Industry Program in Clinical Trial Research and Administration
Bioinformatics Institute of India
C-56A/28, Sector-62, Noida - 201301, U.P. India, Tel.: 120-4320801/802
Industry Program in Clinical Trial, Research & Administration
Distance Participation
Autumn 2006 Batch
Subject: Re-Registration due to non appearance /non-clearance of November 2007 exam
Dear Program Participant,
You have not been able to complete the program due to non-appearance / non clearance of all the papers in November 2007 exam. You can however still complete the programs by re-registering in the next session.
For the same you have to:
1. Submit Re-Registration form and Re-Registration fees Re-registration fees is Rs 5000/- USD 350 only. Re-Registration extends your registration for April 2008 and Nov 2008 examinations. The fees should be paid in the form of demand draft drawn in favour of “Bioinformatics Institute of India” payable at Delhi/New Delhi.
2. Submit exam form and exam fee for the exam in which you wish to appear. Exam fees is Rs 200/- / USD 25 per paper. So if you are to appear in seven papers exam fees will be Rs 1400/- / USD 175 only.
3. Submit Compulsory assignment & Research study (only in the case of non submission of the same earlier). You have to submit the same before April 2008 exam in which you wish to appear.
Please note:-
1. In order to complete Industry Program in Clinical Trial, Research & Administration the participant will have to clear all the seven papers along with the submission of Compulsory assignments and Research Study.
2. To continue in the program, re-registration within notified period is mandatory. If you do not re-register by 31st December 2007, you will not be allowed to continue the program.
3. Participants can submit single Demand draft for re-registration fees and exam fees.
Important Dates:
Last date for re-registration to continue the program
31st December 2007
Last date for Examination form & fee submission for April 2008 exams
28th February 2008
Examination notification for April 2008 exams will be sent in the month of January 2008.
With best wishes,
Program Coordinator
Bioinformatics Institute of India
Enclosure: Re-registration form, Examination Form
BII BLOG: Join the Institute Blog at http://www.biinoida.blogspot.com/ for latest news, lectures, jobs and videos in the field of Bioinformatics, Clinical Trial, Pharma Regulatory Affairs, IPR, Pharma GMP etc.
C-56A/28, Sector-62, Noida - 201301, U.P. India, Tel.: 120-4320801/802
Industry Program in Clinical Trial, Research & Administration
Distance Participation
Autumn 2006 Batch
Subject: Re-Registration due to non appearance /non-clearance of November 2007 exam
Dear Program Participant,
You have not been able to complete the program due to non-appearance / non clearance of all the papers in November 2007 exam. You can however still complete the programs by re-registering in the next session.
For the same you have to:
1. Submit Re-Registration form and Re-Registration fees Re-registration fees is Rs 5000/- USD 350 only. Re-Registration extends your registration for April 2008 and Nov 2008 examinations. The fees should be paid in the form of demand draft drawn in favour of “Bioinformatics Institute of India” payable at Delhi/New Delhi.
2. Submit exam form and exam fee for the exam in which you wish to appear. Exam fees is Rs 200/- / USD 25 per paper. So if you are to appear in seven papers exam fees will be Rs 1400/- / USD 175 only.
3. Submit Compulsory assignment & Research study (only in the case of non submission of the same earlier). You have to submit the same before April 2008 exam in which you wish to appear.
Please note:-
1. In order to complete Industry Program in Clinical Trial, Research & Administration the participant will have to clear all the seven papers along with the submission of Compulsory assignments and Research Study.
2. To continue in the program, re-registration within notified period is mandatory. If you do not re-register by 31st December 2007, you will not be allowed to continue the program.
3. Participants can submit single Demand draft for re-registration fees and exam fees.
Important Dates:
Last date for re-registration to continue the program
31st December 2007
Last date for Examination form & fee submission for April 2008 exams
28th February 2008
Examination notification for April 2008 exams will be sent in the month of January 2008.
With best wishes,
Program Coordinator
Bioinformatics Institute of India
Enclosure: Re-registration form, Examination Form
BII BLOG: Join the Institute Blog at http://www.biinoida.blogspot.com/ for latest news, lectures, jobs and videos in the field of Bioinformatics, Clinical Trial, Pharma Regulatory Affairs, IPR, Pharma GMP etc.
Thursday, November 29, 2007
Bachelors Degree in Bioinformatics
The following are links for some Bioinformatics University and Institutes offereng Bachelors Degree in Bioinformatics - BS Bioinformatics / BSc Bioinformatics
California
Illinois
Massachusetts
Maryland
Michigan
Missouri
New Jersey
New York
Oregon
Pennsylvania
Texas
vss
California
Illinois
Massachusetts
Maryland
Michigan
Missouri
New Jersey
New York
Oregon
Pennsylvania
Texas
vss
National Seminar on e-Security Education through e-Learning, e-Learn 2007
Venue: CDAC (Centre for Development of Advance Computing)
CDAC - B-30 Institutional Area, Sector 62, Noida
Date: 14th December 2007
Details at: http://www.cdacnoida.in/
email: elearn2007@cdacnoida.in
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CDAC - B-30 Institutional Area, Sector 62, Noida
Date: 14th December 2007
Details at: http://www.cdacnoida.in/
email: elearn2007@cdacnoida.in
vss
Wednesday, November 28, 2007
Job Oportunities at Asian Clinical Trials
Job Posting
Asian Clinical Trials (ACT) a division of Suven Life Sciences Limited is a leading CRO in the business of making difference. ACT provides opportunity to explore thought process and ideas and be part of global team working. We reward your commitment and entrepreneur skills and provide excellent opportunity for career advancement.
ACT invites applications for the following positions:
CLINICAL RESEARCH OPERATIONS
1. PROJECT MANAGER
2. CLINICAL TEAM LEADER
3. CLINICAL RESEARCH ASSOCIATE
CLINICAL DATA MANAGEMENT
1. CLINICAL DATA MANAGER
2. DATA VALIDATION ASSOCIATE
3. PROGRAMMER Oracle Clinical
4. SENIOR BIOSTATISTICIAN
Details are available at : http://www.act-india.com/jobposting.htm
Asian Clinical Trials (ACT) a division of Suven Life Sciences Limited is a leading CRO in the business of making difference. ACT provides opportunity to explore thought process and ideas and be part of global team working. We reward your commitment and entrepreneur skills and provide excellent opportunity for career advancement.
ACT invites applications for the following positions:
CLINICAL RESEARCH OPERATIONS
1. PROJECT MANAGER
2. CLINICAL TEAM LEADER
3. CLINICAL RESEARCH ASSOCIATE
CLINICAL DATA MANAGEMENT
1. CLINICAL DATA MANAGER
2. DATA VALIDATION ASSOCIATE
3. PROGRAMMER Oracle Clinical
4. SENIOR BIOSTATISTICIAN
Details are available at : http://www.act-india.com/jobposting.htm
Vb.net
Hey do anybody know how to play songs on button click in vb.net..?
please reply i need it..
thanx in advance
please reply i need it..
thanx in advance
Job Opportunities - Alkem, Sun Pharmaceuticals, Bombay Hospitals, Teva, Regent Drugs
All above opportunities are advertised in TOI November 28, 2007 Ascent
Alkem - Alkem laboratories is a USD 300 mn Indian copany with focus on India, USA, Europe, Canada and many other markets, requires professionals in areas like
Formulation Development, NDDS Development, Formulation Process Development and Optimisation, Analytical Research, API Research, Biotechnology, Food Technology, International Regulatory affairs, Intellectual Property and Bioanalytical
email: hrd@alkem.com Phone: 022-24903045
Bombay Hospitals: Several positions for medical professionals , Nursing Administration and Nursing Teaching Opportunity
email: vyasdp9@yahoo.com
Rx Africal requires Pharmacists with GMP experience
Teva Regent Drugs requires Finance, Production, Technology Transfer, Environment professioanls at Greater Noida / Gajraula
email: hrsupport@pl.rdlmail.com, recruitment@rdlmail.com
Sun Pharmaceutical Requires entry level and marketing professionals all over North India
Alkem - Alkem laboratories is a USD 300 mn Indian copany with focus on India, USA, Europe, Canada and many other markets, requires professionals in areas like
Formulation Development, NDDS Development, Formulation Process Development and Optimisation, Analytical Research, API Research, Biotechnology, Food Technology, International Regulatory affairs, Intellectual Property and Bioanalytical
email: hrd@alkem.com Phone: 022-24903045
Bombay Hospitals: Several positions for medical professionals , Nursing Administration and Nursing Teaching Opportunity
email: vyasdp9@yahoo.com
Rx Africal requires Pharmacists with GMP experience
Teva Regent Drugs requires Finance, Production, Technology Transfer, Environment professioanls at Greater Noida / Gajraula
email: hrsupport@pl.rdlmail.com, recruitment@rdlmail.com
Sun Pharmaceutical Requires entry level and marketing professionals all over North India
Tuesday, November 27, 2007
National Symposium on Systems Biology - Lady Doak College Madurai
National Symposium on Systems Biology
Venue - Lady Doak College Madurai
Date : January 10th, 11th 2008
Organised by Bioinformatics Infrastructure Facility (DBT Sponsored)Department of Biotechnology
Objectives
To analyse the interaction and dynamic changes of molecules within a cell
To identify and measure small molecules, metabolites within a cell or a tissue
To create awareness on protein expression patterns of a cell
Thurst Areas
Bioinformatics, Biomodels, Genetics Network, Transcriptomics, Proteomics, Metabolomics, InteractomicsDetails : Dr R Shenbagarathai, Coordinator
email: systembio08@gmail.com
Phone Number: 0452- 2530527
vss
Venue - Lady Doak College Madurai
Date : January 10th, 11th 2008
Organised by Bioinformatics Infrastructure Facility (DBT Sponsored)Department of Biotechnology
Objectives
To analyse the interaction and dynamic changes of molecules within a cell
To identify and measure small molecules, metabolites within a cell or a tissue
To create awareness on protein expression patterns of a cell
Thurst Areas
Bioinformatics, Biomodels, Genetics Network, Transcriptomics, Proteomics, Metabolomics, InteractomicsDetails : Dr R Shenbagarathai, Coordinator
email: systembio08@gmail.com
Phone Number: 0452- 2530527
vss
Monday, November 26, 2007
Research and Development Proposals
From Harayana State Council for Science and Technology in following areas - Bio-Technology, Health, Food Processing, Waste management, Environment and Energy and other emerging areas.
Further details at www.dstharayana.org
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Further details at www.dstharayana.org
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Walkin Interview - Division of Genetics
Division of Genetics - Indian Agriculture Research Institute
Walkin interviews for project and principal investigators walkin interview at 21.12, details for eligibility etc are available at Hindustan Times Monday November 26
Projects are
Tagging Genes for Resistance to wilt in Lentil - PL Dr H K Dikshit Senior Scientist
Genetic Improvement of soyabean for charcoal rot resistance through molecular techniques : PL Dr Akshay Talukdar Senior Scientist
Mapping of Marker Assisted selection for new genes (Albugo candida) in Indin Mustard PL Dr D K Yadava
vss
Walkin interviews for project and principal investigators walkin interview at 21.12, details for eligibility etc are available at Hindustan Times Monday November 26
Projects are
Tagging Genes for Resistance to wilt in Lentil - PL Dr H K Dikshit Senior Scientist
Genetic Improvement of soyabean for charcoal rot resistance through molecular techniques : PL Dr Akshay Talukdar Senior Scientist
Mapping of Marker Assisted selection for new genes (Albugo candida) in Indin Mustard PL Dr D K Yadava
vss
Financial Assistance for your Innovation
Check Technology Development Board Website www.tdbindia.org for financial assistance in Biotech, Pharma, IT and ITES, Telecom, Chemicals and Agriculture Sector.
Details at Hindustan Times Monday November 26, 2007
visit www.tdbindia.org for project funding guidelines
vss
Details at Hindustan Times Monday November 26, 2007
visit www.tdbindia.org for project funding guidelines
vss
Admission Announcement in Jaipur National University
Jaipur National University which is venture of Seedling Group of Institutions has announced admission for
MPhil and PhD in Life Sciences (Biotechnology, Microbiology and Biochemistry)
MPharma and PhD in Pharmaceutical Sciences
Details are available at http://www.seedlingeducation.com/
email: seedlingacademy@hotmail.com
Last Date: 20th December 2007
vss
MPhil and PhD in Life Sciences (Biotechnology, Microbiology and Biochemistry)
MPharma and PhD in Pharmaceutical Sciences
Details are available at http://www.seedlingeducation.com/
email: seedlingacademy@hotmail.com
Last Date: 20th December 2007
vss
Saturday, November 24, 2007
FICCI - Cygnus White Paper on Clinical Trials
http://www.cygnusindia.com/White%20Paper%20on%20Global%20Clinical%20Trials%20in%20India%20-%20Prospects%20a.pdf
The above is a high quality report, though published in 2005. Please note that it mentions Bioinformatics Institute of India as an importatn institution providing Clinical Trial Training
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The above is a high quality report, though published in 2005. Please note that it mentions Bioinformatics Institute of India as an importatn institution providing Clinical Trial Training
vss
Employment Opportunities at SRL Ranbaxy
SRL Ranbaxy Employment Opportunities
As part of our growth plans, we have immediate requirement of following professionals.
Following positions are currently available:
Pathologist
Sr. Scientific Officers
Scientific Officer
Manager - HR
Regional Sales Manager
Area Sales Managers
Sales Officers
Vacancies at R&D
Research Officer
As part of our growth plans, we have immediate requirement of following professionals.
Following positions are currently available:
Pathologist
Sr. Scientific Officers
Scientific Officer
Manager - HR
Regional Sales Manager
Area Sales Managers
Sales Officers
Vacancies at R&D
Research Officer
WIPRO White Papers on Health Care
Check the following link for WIPRO White Papers on Health care
Parallel implementation of biological software tools with NCBI’s blast as an example to achieve "load balancing"
HIPAA and clinical research
Whitepaper on HIPAA
Data mining: Mining for gold
Data quality - A problem and an approach
Choosing the right BSP
Enhancing end customer service delivery
Outsourcing : Total cost of management benefits
BII Admin
Parallel implementation of biological software tools with NCBI’s blast as an example to achieve "load balancing"
HIPAA and clinical research
Whitepaper on HIPAA
Data mining: Mining for gold
Data quality - A problem and an approach
Choosing the right BSP
Enhancing end customer service delivery
Outsourcing : Total cost of management benefits
BII Admin
Career Prospects in Clinical Research and Regulatory Affairs
CAREER PROSPECTS
2,50,000 vacancies available worldwide
50,000 job openings in India by 2010*
Highest remuneration packages owing to the shortage of skilled professionals
Segment wise opportunities
Doctors
Principal Investigator
Co-investigator
Medical Advisor
Drug Developers
Regulatory Affairs Manager and
Clinical Research Physician
Para Medics, Pharmacists and Life Sciences Graduates
Medical Writers
Clinical Research Associates
Site Co-ordinators
Clinical Research Managers and
Drug Development Associates
Head of Research
Management Professionals
Business Development
Clinical Project Management
Clinical Research Management and
Regulatory Affairs Management
CEO / Head of Organisation
*Source: McKinsey Report
2,50,000 vacancies available worldwide
50,000 job openings in India by 2010*
Highest remuneration packages owing to the shortage of skilled professionals
Segment wise opportunities
Doctors
Principal Investigator
Co-investigator
Medical Advisor
Drug Developers
Regulatory Affairs Manager and
Clinical Research Physician
Para Medics, Pharmacists and Life Sciences Graduates
Medical Writers
Clinical Research Associates
Site Co-ordinators
Clinical Research Managers and
Drug Development Associates
Head of Research
Management Professionals
Business Development
Clinical Project Management
Clinical Research Management and
Regulatory Affairs Management
CEO / Head of Organisation
*Source: McKinsey Report
Job Requirement at Jubiliant Biosys
Job Requirements at Jubiliant Biosys
Scientist - Ph.D in Organic / Pharmaceutical Sciences ( R&D )
Officer/Executive - Sales Administration (Consumer Products Division)
Asstt.Manager/Deputy Manager - Commercial & Accounting
Associates Biochemistry
Associates Cell Biology
Senior Scientist Biochemistry
Senior Scientist Cell Biology
Senior Scientist High Through-Put screen (HTS)
Scientist
Scientist (Biochemistry)
Sr.Scientist / Scientist
Scientist (Analytical Chemistry)
Scientist (Data Management)
Manager Business Development / Sr.Manager
.net Sr.Software Engineer
Intellectual Property Management
Scientist (Invivo PK)
System Administrator
Scientist (Oncology)
Scientist (Metabolic Disorder)
Scientist -Toxicology
Project Manager
Sr. Scientist
Project Manager
Click the above links for details
Scientist - Ph.D in Organic / Pharmaceutical Sciences ( R&D )
Officer/Executive - Sales Administration (Consumer Products Division)
Asstt.Manager/Deputy Manager - Commercial & Accounting
Associates Biochemistry
Associates Cell Biology
Senior Scientist Biochemistry
Senior Scientist Cell Biology
Senior Scientist High Through-Put screen (HTS)
Scientist
Scientist (Biochemistry)
Sr.Scientist / Scientist
Scientist (Analytical Chemistry)
Scientist (Data Management)
Manager Business Development / Sr.Manager
.net Sr.Software Engineer
Intellectual Property Management
Scientist (Invivo PK)
System Administrator
Scientist (Oncology)
Scientist (Metabolic Disorder)
Scientist -Toxicology
Project Manager
Sr. Scientist
Project Manager
Click the above links for details
Thursday, November 22, 2007
Complaint
This is strange. I enrolled into the Industry program BI in Jan 2007 and I haven't been able to login at the BII website. I have written heaps of mails and called them a dozen times!! This is really sad!!
Wednesday, November 21, 2007
Put Your Professional Profiles
Dear Blog Members
BII continuosly receives enquiries from employers about suitable candidates. We are planning to have a zone on this Blog where we will have professional profiles of our members for companies to view. We therefore request all the interested members to post their resumes on the blog and we will manage them in a new link
The resumes can be submitted in the form of new post
vss
BII continuosly receives enquiries from employers about suitable candidates. We are planning to have a zone on this Blog where we will have professional profiles of our members for companies to view. We therefore request all the interested members to post their resumes on the blog and we will manage them in a new link
The resumes can be submitted in the form of new post
vss
Good Info on Pharma Regulatory Affairs
REGULATORY AFFAIRSDrug industry relies on those who navigate the ground between development and approval
CORINNE A. MARASCO, C&EN WASHINGTON
The pharmaceutical industry is the most regulated of all industries. Think of any drug on the market today to treat a disease, a chronic condition, or even something as mundane--and confounding--as the common cold. No drug would be available without the teams of medical researchers and other specialists who worked to make sure it received Food & Drug Administration approval.
Regulatory affairs professionals are key, but perhaps overlooked, players in drug development. They are the primary communications link between the company and agencies such as FDA, and they are responsible for keeping up with the increasing scope and complexity of regulations both here and abroad.
In the pharmaceutical industry, regulatory affairs professionals have expertise in the legal and regulatory environments, as well as in clinical research protocols. They are the primary interpreters of the laws and regulations for other members of the company's R&D, manufacturing, and compliance staff. Regulatory affairs professionals must have a thorough understanding of the complex set of regulations within which FDA operates: 21 CFR (Code of Federal Regulations), Sections 1 through 1299. They also need to be familiar with regulations promulgated by a whole range of agencies: the Environmental Protection Agency, Federal Trade Commission, Occupational Safety & Health Administration, and Drug Enforcement Administration.
A good regulatory professional must also be aware of the subtleties of regulations worldwide. Keeping up-to-date on regulations is essential in regulatory affairs; changes in regulations can affect the clinical trials process, regulatory strategy, decisions on what kinds of trials are needed, and so forth. New areas evolve as science changes, so time is spent tracking changes in regulations all over the world. The stakes can be high; drug approvals--as well as delays or failures--are featured prominently in the media and can make or break a company.
Although the work emphasizes regulatory knowledge, it's not just for wonks. Scientific training is also valued and helpful. "Employers are looking for people who understand the science that's driving the process," says Sherry Keramidas, executive director of the Regulatory Affairs Professional Society. "Understanding the clinical process and some of the challenges of clinical care helps regulatory affairs professionals understand the clinical trials process and what is or is not possible," she explains.
Bonnie Charpentier, a Ph.D. chemist and vice president of regulatory affairs at Genitope, agrees. "The field of regulatory affairs has become increasingly more science- and issue-based and less rote and bureaucratic, as the speed of the pharmaceutical and biologics development has increased and the science has become more complex. A regulatory professional now spends more time on substantive scientific and medical issues and on planning for the experiments and clinical studies to achieve approval.
"Currently there is a need for regulatory professionals," Charpentier says. "To do the job well requires one to be a generalist, comfortable working across a range of scientific disciplines, and competent in asking questions and defining answers."
For more info click http://pubs.acs.org/cen/employment/8048/8048regulatoryaffairs.html
CORINNE A. MARASCO, C&EN WASHINGTON
The pharmaceutical industry is the most regulated of all industries. Think of any drug on the market today to treat a disease, a chronic condition, or even something as mundane--and confounding--as the common cold. No drug would be available without the teams of medical researchers and other specialists who worked to make sure it received Food & Drug Administration approval.
Regulatory affairs professionals are key, but perhaps overlooked, players in drug development. They are the primary communications link between the company and agencies such as FDA, and they are responsible for keeping up with the increasing scope and complexity of regulations both here and abroad.
In the pharmaceutical industry, regulatory affairs professionals have expertise in the legal and regulatory environments, as well as in clinical research protocols. They are the primary interpreters of the laws and regulations for other members of the company's R&D, manufacturing, and compliance staff. Regulatory affairs professionals must have a thorough understanding of the complex set of regulations within which FDA operates: 21 CFR (Code of Federal Regulations), Sections 1 through 1299. They also need to be familiar with regulations promulgated by a whole range of agencies: the Environmental Protection Agency, Federal Trade Commission, Occupational Safety & Health Administration, and Drug Enforcement Administration.
A good regulatory professional must also be aware of the subtleties of regulations worldwide. Keeping up-to-date on regulations is essential in regulatory affairs; changes in regulations can affect the clinical trials process, regulatory strategy, decisions on what kinds of trials are needed, and so forth. New areas evolve as science changes, so time is spent tracking changes in regulations all over the world. The stakes can be high; drug approvals--as well as delays or failures--are featured prominently in the media and can make or break a company.
Although the work emphasizes regulatory knowledge, it's not just for wonks. Scientific training is also valued and helpful. "Employers are looking for people who understand the science that's driving the process," says Sherry Keramidas, executive director of the Regulatory Affairs Professional Society. "Understanding the clinical process and some of the challenges of clinical care helps regulatory affairs professionals understand the clinical trials process and what is or is not possible," she explains.
Bonnie Charpentier, a Ph.D. chemist and vice president of regulatory affairs at Genitope, agrees. "The field of regulatory affairs has become increasingly more science- and issue-based and less rote and bureaucratic, as the speed of the pharmaceutical and biologics development has increased and the science has become more complex. A regulatory professional now spends more time on substantive scientific and medical issues and on planning for the experiments and clinical studies to achieve approval.
"Currently there is a need for regulatory professionals," Charpentier says. "To do the job well requires one to be a generalist, comfortable working across a range of scientific disciplines, and competent in asking questions and defining answers."
For more info click http://pubs.acs.org/cen/employment/8048/8048regulatoryaffairs.html
International Bioinformatics Conferences
Nov 26, 2007
United States - CA
Search and Knowledge Building for Biological Datasets
Nov 28, 2007
Australia - Vic
ISSNIP International Workshop on Biomedical Informatics
Nov 30, 2007
United States - Colorado
Rocky Mountain Bioinformatics Conference
Nov 30, 2007
United States - CA
RECOMB Satellite Workshop on Systems Biology
Dec 03, 2007
France
International Workshop on Web Data Integration and Mining for Life Sciences
Dec 03, 2007
United States - NY
DREAM2: The 2nd Dialogue on Reverse Engineering Assessment and Methods
Dec 03, 2007
Singapore
The 18th International Conference on Genome Informatics (GIW 2007)
Dec 03, 2007
United Kingdom - Oxfordshire
Molecular Evolution and Comparative Genomics
Dec 06, 2007
Singapore
2nd International Symposium on Languages in Biology and Medicine (LBM) 2007
Dec 07, 2007
Canada - BC
New Problems and Methods in Computational Biology
Dec 10, 2007
Australia - QLD
2007 International Symposium on Computational Models for Life Sciences
Dec 13, 2007
Spain
CAMDA07
Dec 13, 2007
United States - Ohio
2007 Workshop on Machine Learning Methods in Biomedicine and Bioinformatics
Jan 04, 2008
United States - HI
PSB 2008 - Pacific Symposium on Biocomputing
Jan 04, 2008
United States - Hawaii
Multiscale Modeling and Simulation: from Molecules to Cells to Organisms
Jan 05, 2008
United States - CA
Genetic Analyis: model organisms to human biology 2
Jan 14, 2008
Japan
The Sixth Asia-Pacific Bioinformatics Conference (APBC2008)
Jan 25, 2008
Mexico - Mexico
4th WSEAS Int.Conf. on MATHEMATICAL BIOLOGY and ECOLOGY (MABE’08)
Jan 28, 2008
Portugal
BIOSIGNALS 2008 - International Conference on Bio-inspired Systems and Signal Processing
Feb 02, 2008
United States - CA
Joint Meeting of the Biophysical Society 52nd Annual Meeting and 16th International Biophysics Congress
Mar 04, 2008
Spain
2008 International Workshop on Intelligent Informatics in Biology and Medicine (IIBM 2008)
Mar 05, 2008
United States - MA
Conference on Semantics in Healthcare & Life Sciences (C-SHALS)
Mar 10, 2008
Italy - TN
CoSBi Computational and Systems Biology Course
Mar 10, 2008
United States - CA
2008 AMIA Summit on Translational Bioinformatics
Mar 16, 2008
Brazil
Bioinformatics Track @ ACM Symposium on Applied Computing (SAC) 2008
Mar 25, 2008
France - Paris
Brain Diseases and Molecular Machines: Spotlights from Evolution, Development and Network Biology
Mar 26, 2008
Italy
European Conference on Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics 2008
Mar 30, 2008
Singapore
12th Annual International Conference on Research in Computational Molecular Biology (RECOMB2008)
Apr 14, 2008
United States - FL
HiCOMB 2008
Apr 19, 2008
China - Guangdong Provin
BIT’S Peptide and Protein Conference
Apr 20, 2008
United States - WA
Systems Biology and Engineering, 7th Annual International Symposium
May 06, 2008
United States - GA
ISBRA 2008: 4-th International Symposium on Bioinformatics Research and Applications
May 18, 2008
Turkey
International Symposium on Health Informatics and Bioinformatics (HIBIT ’08)
Jun 01, 2008
United States
2008 FASEB Summer Research Conference
Jun 12, 2008
China - Shanghai
World Cancer Congress-2008
Jun 14, 2008
Italy
Lipari International Summer School on BioInformatics and Computational Biology - Biological Networks: Evolution, Interaction and Computation
Jun 25, 2008
France
DILS 2008: 5th International Workshop on Data Integration in the Life Sciences
Jul 07, 2008
United States - FL
International Conference on Bioinformatics, Computational Biology, Genomics and Chemoinformatics
Jul 07, 2008
Austria
BIRD’08 - 2nd International Conference on Bioinformatics Research and Development
Jul 18, 2008
Canada
ISMB 2008
Sep 09, 2008
Germany
German Conference on Bioinformatics
Sep 14, 2008
Australia - NSW
WATOC 2008
Sep 15, 2008
Italy
Mini EURO Conference on Computational Biology, Bioinformatics and Medicine
Sep 22, 2008
Italy -
ECCB’08 (European Conference on Computational Biology)
Oct 07, 2008
South Korea
The 9th International Congress on Cell Biology (ICCB)
Sep 18, 2009
Mauritius
International Conference on Biotechnology and Bioinformatics
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United States - CA
Search and Knowledge Building for Biological Datasets
Nov 28, 2007
Australia - Vic
ISSNIP International Workshop on Biomedical Informatics
Nov 30, 2007
United States - Colorado
Rocky Mountain Bioinformatics Conference
Nov 30, 2007
United States - CA
RECOMB Satellite Workshop on Systems Biology
Dec 03, 2007
France
International Workshop on Web Data Integration and Mining for Life Sciences
Dec 03, 2007
United States - NY
DREAM2: The 2nd Dialogue on Reverse Engineering Assessment and Methods
Dec 03, 2007
Singapore
The 18th International Conference on Genome Informatics (GIW 2007)
Dec 03, 2007
United Kingdom - Oxfordshire
Molecular Evolution and Comparative Genomics
Dec 06, 2007
Singapore
2nd International Symposium on Languages in Biology and Medicine (LBM) 2007
Dec 07, 2007
Canada - BC
New Problems and Methods in Computational Biology
Dec 10, 2007
Australia - QLD
2007 International Symposium on Computational Models for Life Sciences
Dec 13, 2007
Spain
CAMDA07
Dec 13, 2007
United States - Ohio
2007 Workshop on Machine Learning Methods in Biomedicine and Bioinformatics
Jan 04, 2008
United States - HI
PSB 2008 - Pacific Symposium on Biocomputing
Jan 04, 2008
United States - Hawaii
Multiscale Modeling and Simulation: from Molecules to Cells to Organisms
Jan 05, 2008
United States - CA
Genetic Analyis: model organisms to human biology 2
Jan 14, 2008
Japan
The Sixth Asia-Pacific Bioinformatics Conference (APBC2008)
Jan 25, 2008
Mexico - Mexico
4th WSEAS Int.Conf. on MATHEMATICAL BIOLOGY and ECOLOGY (MABE’08)
Jan 28, 2008
Portugal
BIOSIGNALS 2008 - International Conference on Bio-inspired Systems and Signal Processing
Feb 02, 2008
United States - CA
Joint Meeting of the Biophysical Society 52nd Annual Meeting and 16th International Biophysics Congress
Mar 04, 2008
Spain
2008 International Workshop on Intelligent Informatics in Biology and Medicine (IIBM 2008)
Mar 05, 2008
United States - MA
Conference on Semantics in Healthcare & Life Sciences (C-SHALS)
Mar 10, 2008
Italy - TN
CoSBi Computational and Systems Biology Course
Mar 10, 2008
United States - CA
2008 AMIA Summit on Translational Bioinformatics
Mar 16, 2008
Brazil
Bioinformatics Track @ ACM Symposium on Applied Computing (SAC) 2008
Mar 25, 2008
France - Paris
Brain Diseases and Molecular Machines: Spotlights from Evolution, Development and Network Biology
Mar 26, 2008
Italy
European Conference on Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics 2008
Mar 30, 2008
Singapore
12th Annual International Conference on Research in Computational Molecular Biology (RECOMB2008)
Apr 14, 2008
United States - FL
HiCOMB 2008
Apr 19, 2008
China - Guangdong Provin
BIT’S Peptide and Protein Conference
Apr 20, 2008
United States - WA
Systems Biology and Engineering, 7th Annual International Symposium
May 06, 2008
United States - GA
ISBRA 2008: 4-th International Symposium on Bioinformatics Research and Applications
May 18, 2008
Turkey
International Symposium on Health Informatics and Bioinformatics (HIBIT ’08)
Jun 01, 2008
United States
2008 FASEB Summer Research Conference
Jun 12, 2008
China - Shanghai
World Cancer Congress-2008
Jun 14, 2008
Italy
Lipari International Summer School on BioInformatics and Computational Biology - Biological Networks: Evolution, Interaction and Computation
Jun 25, 2008
France
DILS 2008: 5th International Workshop on Data Integration in the Life Sciences
Jul 07, 2008
United States - FL
International Conference on Bioinformatics, Computational Biology, Genomics and Chemoinformatics
Jul 07, 2008
Austria
BIRD’08 - 2nd International Conference on Bioinformatics Research and Development
Jul 18, 2008
Canada
ISMB 2008
Sep 09, 2008
Germany
German Conference on Bioinformatics
Sep 14, 2008
Australia - NSW
WATOC 2008
Sep 15, 2008
Italy
Mini EURO Conference on Computational Biology, Bioinformatics and Medicine
Sep 22, 2008
Italy -
ECCB’08 (European Conference on Computational Biology)
Oct 07, 2008
South Korea
The 9th International Congress on Cell Biology (ICCB)
Sep 18, 2009
Mauritius
International Conference on Biotechnology and Bioinformatics
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Tuesday, November 20, 2007
Clinical Trial Registry
NEW DELHI: Clinical trials conducted for testing efficacy of new drugs are set to become transparent with the launch of a national registry for recording such an exercise. The Clinical Trials Registry - India (CTRI), the first such initiative in Asia, was launched at the Indian Council of Medical Research (ICMR) here on Friday. Any researcher who plans to conduct drug trials on humans is expected to declare the details of the exercise in the Registry, that is jointly funded by the Department of Science and Technology, WHO and ICMR. Such prospective registration of clinical trials in humans before enrolling the first participant, and making sufficient information of ongoing research available to all those involved in healthcare decision making is now a national and international priority. "With the launch of this registry, India will be among the few select countries like Australia, UK and the US that are making researchers accountable through public disclosure," N K Ganguly, ICMR Director-General said. The objective is to restore public confidence in clinical research, which was being coed in some parts of the country in an hush-hush manner. "The CTRI will ensure that a complete view of ongoing research is available at the click of a mouse," Ganguly said. Twenty items that meet the requirement of the WHO International Clinical Trials Registry Platform will have to be declared at the time of registration. Only trials properly registered will be considered for publication in international research journals.
Bioinformatics Centre University of Pune
JOINT WORKSHOP
on
Knowledge Discovery In Life Sciences: Modeling of Small Molecules to Macromolecules
December 11 - December 17, 2007
at
Bioinformatics CentreUniversity of PunePune 411 007
Sponsored by
Department of BiotechnologyGovernment of India
&
Bioinformatics Centre @ University of Pune
Details at : http://bioinfo.ernet.in/workshopdec07/
on
Knowledge Discovery In Life Sciences: Modeling of Small Molecules to Macromolecules
December 11 - December 17, 2007
at
Bioinformatics CentreUniversity of PunePune 411 007
Sponsored by
Department of BiotechnologyGovernment of India
&
Bioinformatics Centre @ University of Pune
Details at : http://bioinfo.ernet.in/workshopdec07/
TCS Clinical Trial Management Solution - Clin e2e
Clin-e2eTM is an end-to-end solution that addresses all four phases of clinical trials. Apart from
having a user-friendly navigation during Trial Design, Trial Set-up, Trial Conduct and Trial Closure, Clin-e2e provides a secure onlineenvironment for Electronic Data
Capture and integrates siteslabs with sponsors. Pharma companies benefi t from faster
creation of customized CRFs; easy evaluation and investigation of subjects; eff ective capture
of the subject’s history, review and investigation details; comprehensive audit trail; and
effi cient contract management.
What makes Clin-e2eTM unique
Protocol Driven – Ensures in-built validation across
the entire Data Management Process and Compliance
Flexible – Handle both paper-based trials and
electronic data capture
Universal Clinical Repository – Allows creation of
CRF Repository and Study Templates, that can be reused,
thereby reducing the Study time
Workfl ow – Role based query management workfl ow
for data modifi cation and correction
Interfaces – Readily available interface to integrate
with industry standard products like Documentum,
MedDRA and SAS and other third-party enterprise
systems
Regulatory Compliant – Compliant with is 21 CFR
Part 11, GCP
Data Standards based – Meets the CDISC ODM and
SDTM Standards
Further Details about Clin e2e can be obtained from TCS
About Life Sciences & Healthcare Practice
TCS’ Life Sciences & Healthcare (LSHC) Industry Practice, provides
IT services and solutions to companies in medical research,
pharmaceutical, healthcare and medical devices industries.
Solutions include Computational Biology & Drug Discovery Services
for the Life Sciences industry; Clinical Trial Management, Clinical
Data Management, Manufacturing & Sales Force Automation for
Pharma companies; Electronic Medical Records, Telemedicine &
Hospital Management for the Healthcare sector; and Application
Development & Maintenance for companies in the Medical Devices
business.
For more information visit www.tcs.com/healthcare
Visual Report on effect of Meditation on Brain
Those interested may check up Times of India Page 21, November 20 2007
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Clinical Trials Market to Grow at 15 % : ICRI
The $ 300 clinical trials market is expected to grow at an annual growth rate of 15 % over the next 4 years at top official of Institute of Clinical Research India (ICRI) said. This will bring nearly 15 % of total global clinical trials to Indiaby 2011 and will generate an annual revenue of $ 1 billion, ICRI's Chief Executive Officer Antony Woodman Said "Currently there are 268 approved clinical trials in India, as compared to a global total of 180,000. The value of current clinical trials in India is $ 300 million" he said. However a lack of competent personnel in the country and appropriate research infrastructure are posing major challenges to rowth, woodman said
Source Economic Times Monday November 19 New Delhi
Source Economic Times Monday November 19 New Delhi
Monday, November 19, 2007
Seminar on Pharma Product Life Cycle
Optimising Pharma Product Lifecycle : Revitalising The "Cash Cow" (Intermediate - Advanced Level )
Enhancing product life cycle management through development and implementation of innovative, dynamic and responsive product management strategies
3rd - 4th December 2007
Singapore
LAST OPPORTUNITY TO REGISTER!!!
Optimising Pharma Product Lifecycle : Revitalising The "Cash Cow" (Intermediate - Advance) aims to equip you with effective product portfolio strategies, creative approaches in brand loyalty building, effective marketing ROI econometric models, new line extension strategies and effective portfolio management to maximize sales figures.
Our international course trainer, Professor Carolyn Choh Fleming, is the Professor of Pharmaceutical Marketing at Saint Joseph's University's Executive Pharma Marketing MBA, Philadelphia, USA. She joined Saint Joseph's after a 15- year career in sales and marketing both domestically and globally, primarily in the pharmaceutical industry. Her experience in pharmaceuticals ranges from sales at Rhone Poulenc Rorer (now Sanofi-Aventis) and marketing at Forest Labs, Wyeth, and Gynétics. Some of the multinationals currently utilizing her services include Abbott, Rototech, Cytogen, Novartis, Ferring, Eisai and King Pharmaceuticals.
Regional case studies will be presented by Jasmine Hoo, Business Unit Director of Bristol-Myers Squibb, Singapore.
You and your organization will gain crucial insights into:
Identifying strategies to optimize product lifecycle
Identifying ways to generate extraordinary business in the changing & challenging pharmaceutical industry
Learning what you need to do to ensure outstanding launch success
Developing a brand asset development program
Selecting areas for ROI attention
Identifying the elements to create a customer centric business
Developing an effective maturity strategy
Strategising ways to improve product management in your organization
Discovering the best practice in product lifecycle strategy and operation
Benchmarking product management in your organisation to best practices in the industry
For the registration form, please use the following link:
http://www.marcusevansassets.com/doc/pdfs/Ep_11331.pdf
If the link is inaccessible, please reply my mail, and I will reply as soon as possible.
To register, simply fill out the registration form with credit card details, attention it to Karyn Nair and fax it to +603 2723 6622.
Take advantage of the 10% discount by registering 3 or more delegates.
Best Regards,
Karyn Nair
Marketing Executive
marcus evans
Telephone : +(603) 2723 6611
Fax : +(603) 2723 6622
Email : karynn@marcusevanskl.com
19955850If you no longer wish to receive further marketing e-mails, please click here
Enhancing product life cycle management through development and implementation of innovative, dynamic and responsive product management strategies
3rd - 4th December 2007
Singapore
LAST OPPORTUNITY TO REGISTER!!!
Optimising Pharma Product Lifecycle : Revitalising The "Cash Cow" (Intermediate - Advance) aims to equip you with effective product portfolio strategies, creative approaches in brand loyalty building, effective marketing ROI econometric models, new line extension strategies and effective portfolio management to maximize sales figures.
Our international course trainer, Professor Carolyn Choh Fleming, is the Professor of Pharmaceutical Marketing at Saint Joseph's University's Executive Pharma Marketing MBA, Philadelphia, USA. She joined Saint Joseph's after a 15- year career in sales and marketing both domestically and globally, primarily in the pharmaceutical industry. Her experience in pharmaceuticals ranges from sales at Rhone Poulenc Rorer (now Sanofi-Aventis) and marketing at Forest Labs, Wyeth, and Gynétics. Some of the multinationals currently utilizing her services include Abbott, Rototech, Cytogen, Novartis, Ferring, Eisai and King Pharmaceuticals.
Regional case studies will be presented by Jasmine Hoo, Business Unit Director of Bristol-Myers Squibb, Singapore.
You and your organization will gain crucial insights into:
Identifying strategies to optimize product lifecycle
Identifying ways to generate extraordinary business in the changing & challenging pharmaceutical industry
Learning what you need to do to ensure outstanding launch success
Developing a brand asset development program
Selecting areas for ROI attention
Identifying the elements to create a customer centric business
Developing an effective maturity strategy
Strategising ways to improve product management in your organization
Discovering the best practice in product lifecycle strategy and operation
Benchmarking product management in your organisation to best practices in the industry
For the registration form, please use the following link:
http://www.marcusevansassets.com/doc/pdfs/Ep_11331.pdf
If the link is inaccessible, please reply my mail, and I will reply as soon as possible.
To register, simply fill out the registration form with credit card details, attention it to Karyn Nair and fax it to +603 2723 6622.
Take advantage of the 10% discount by registering 3 or more delegates.
Best Regards,
Karyn Nair
Marketing Executive
marcus evans
Telephone : +(603) 2723 6611
Fax : +(603) 2723 6622
Email : karynn@marcusevanskl.com
19955850If you no longer wish to receive further marketing e-mails, please click here
Urging all Blog Members
Dear Members
We wish to make this a lively and a vibrant blog. We urge each of the members to post at-least one relevant news, view, event annoucement etc every month. This contribution from each of the members will take this blog to a new height.
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We wish to make this a lively and a vibrant blog. We urge each of the members to post at-least one relevant news, view, event annoucement etc every month. This contribution from each of the members will take this blog to a new height.
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Sunday, November 18, 2007
Best Wishes for November 25 and 25 Exams
On Behalf of BII Institute Faculty, Staff and Management we wish "ALL THE BEST" students appearing in the November Examinations.
We are sure that the completion of the BII Program in your choosen area will take your career to new soaring heights.
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We are sure that the completion of the BII Program in your choosen area will take your career to new soaring heights.
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To Join this Blog
If you wish to join this blog as member and post your own related topics then mail us and provide your id at - members@bioinformaticscentre.org
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Biology and Medicine in the 21st Century Lecture
Biology and Medicine in the 21st Century Lecture
By Prof Eric Lander , Direct Broad Institute of MIT and Harvard
Engineering the Immune System
By Prof David Baltimore, Nobel Laureate in Physiology or Medicine
19th Novemeber 2007, 2:30 PM
National Institute of Immunology at Aruna Asaf Ali Marg , New Delhi
All Are Cordially Invited, details at TOI Nov 18 Pg 2
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By Prof Eric Lander , Direct Broad Institute of MIT and Harvard
Engineering the Immune System
By Prof David Baltimore, Nobel Laureate in Physiology or Medicine
19th Novemeber 2007, 2:30 PM
National Institute of Immunology at Aruna Asaf Ali Marg , New Delhi
All Are Cordially Invited, details at TOI Nov 18 Pg 2
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Saturday, November 17, 2007
PhD Program NCL Pune / Jobs at ICMR / Jobs at ICAR
Last Date 6th December 2007, Advt TOI November 16 Pg 25
Details at http://www.ncl-india.org/ncljobs/managejobs.asp
Research Associate ICMR Advt TOI November 16 Pg 25
PHD with 3 years of doctoral research exp in Lif Science / Biological Sciences
National Bureau of Plant Genetic Resources / Indian Council of Agriculture Research Several Posts
Walk in Interview in New Delhi 26/11/2007 TOI November 16 Pg 25
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Details at http://www.ncl-india.org/ncljobs/managejobs.asp
Research Associate ICMR Advt TOI November 16 Pg 25
PHD with 3 years of doctoral research exp in Lif Science / Biological Sciences
National Bureau of Plant Genetic Resources / Indian Council of Agriculture Research Several Posts
Walk in Interview in New Delhi 26/11/2007 TOI November 16 Pg 25
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Friday, November 16, 2007
Make maximum use of the blog
We urge all the memebers of this blog to use this at its fullest. It can be used to post news, jobs, careers, querries etc. Users can also share their thoughts , writeups etc here. Every one is encouraged to post comment and participate
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Infosys Life Science White Paper and Case Study Links
White Papers
Read the Infosys White Paper, "How Plasma Therapeutics Leverage IT to Transform Drug Discovery" [PDF]
Read the Infosys White Paper, "Objective measurable criteria for clinical trial management" [PDF]
Read the Infosys White Paper, "The Life Sciences Challenge : An Industry Under Pressure to Innovate" [PDF]
Case Studies
Global CRO Streamlines Project Management, Cuts Clinical Trial Lead Time Read more
Service Transformation Cuts Application Lifecycle Management Cost by 30% for Global Pharmaceutical Leader Read more
Virtual Predictive Tool Rationalizes Lead Compound Identification for New Drug Discovery Read more
Reengineered and Automated 21 CFR Part 11 Compliant Business Processes for a Leading CRO Read more
Infosys' Data Management System Aids Crop Seed Selection Read more
Developing a Document Management System for a Pharmaceuticals giant Read more
Oracle Clinical Implementation for CRO Read more
Increasing productivity for a Drug Discovery Company Read more
Business Intelligence for enhanced performance tracking Read more
Improving IT Efficiencies for an Agribusiness Giant Read more
Portal for ECG test data dissemination Read more
Web based application for protein modeling Read more
High throughput screening for small molecules binding to target active site Read more
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Read the Infosys White Paper, "How Plasma Therapeutics Leverage IT to Transform Drug Discovery" [PDF]
Read the Infosys White Paper, "Objective measurable criteria for clinical trial management" [PDF]
Read the Infosys White Paper, "The Life Sciences Challenge : An Industry Under Pressure to Innovate" [PDF]
Case Studies
Global CRO Streamlines Project Management, Cuts Clinical Trial Lead Time Read more
Service Transformation Cuts Application Lifecycle Management Cost by 30% for Global Pharmaceutical Leader Read more
Virtual Predictive Tool Rationalizes Lead Compound Identification for New Drug Discovery Read more
Reengineered and Automated 21 CFR Part 11 Compliant Business Processes for a Leading CRO Read more
Infosys' Data Management System Aids Crop Seed Selection Read more
Developing a Document Management System for a Pharmaceuticals giant Read more
Oracle Clinical Implementation for CRO Read more
Increasing productivity for a Drug Discovery Company Read more
Business Intelligence for enhanced performance tracking Read more
Improving IT Efficiencies for an Agribusiness Giant Read more
Portal for ECG test data dissemination Read more
Web based application for protein modeling Read more
High throughput screening for small molecules binding to target active site Read more
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Careers at VIMTA Labs Limited
About VIMTA Labs
ould you like to be a part of an organization that is devoted to excellence in quality and uncompromising integrity in its service? If yes, read on. In our fervor to realize our vision, we are looking for talented, experienced professionals who have a taste for excellence and who never want to stop learning. As a multi disciplinary scientific organization, VIMTA gives its people an experience in a variety of scientific fields. We encourage our people to constantly improve their knowledge and skills and to this end we conduct ongoing training programs in various ways. VIMTA is an equal opportunity employer and provides excellent working environment with competitive salaries commensurate with experience and education.
Career Opportunities
Our current career opportunities: Manager / Group Leader (Analytical)- Ref Code: VLL/01 Scientist (Analytical)- Ref Code: VLL/02 Manager / Group Leader (Bioanalytical)- Ref Code: VLL/03 Group Leader / Scientist (Peptide Synthesis)- Ref Code: VLL/04 Scientist / Engineer (Environment)- Ref Code: VLL/05 Manager - Marketing (Environment)- Ref Code: VLL/06 Clinical Biochemist- Ref Code: VLL/07
E-mail your resumes to: careers@vimta.com
vss
ould you like to be a part of an organization that is devoted to excellence in quality and uncompromising integrity in its service? If yes, read on. In our fervor to realize our vision, we are looking for talented, experienced professionals who have a taste for excellence and who never want to stop learning. As a multi disciplinary scientific organization, VIMTA gives its people an experience in a variety of scientific fields. We encourage our people to constantly improve their knowledge and skills and to this end we conduct ongoing training programs in various ways. VIMTA is an equal opportunity employer and provides excellent working environment with competitive salaries commensurate with experience and education.
Career Opportunities
Our current career opportunities: Manager / Group Leader (Analytical)- Ref Code: VLL/01 Scientist (Analytical)- Ref Code: VLL/02 Manager / Group Leader (Bioanalytical)- Ref Code: VLL/03 Group Leader / Scientist (Peptide Synthesis)- Ref Code: VLL/04 Scientist / Engineer (Environment)- Ref Code: VLL/05 Manager - Marketing (Environment)- Ref Code: VLL/06 Clinical Biochemist- Ref Code: VLL/07
E-mail your resumes to: careers@vimta.com
vss
Thursday, November 15, 2007
About Bioinformatics Institute of India
Bioinformatics Institute of India, has been setup as a premier Bioinformatics society, for the promotion, growth and prosperity of bioinformatics sciences. The institute has been promoted as a non profit making educational, R&D and development centre of bioinformatics. The aim and vision of the institute is to provide a platform for individuals, professionals, R&D Organisations, Pharmaceutical & Software companies to utilize and harness the Indian bioinformatics potential.
The institute aims not only educational and research initiative in this direction but also vouch for creating a talent pool of professionals from various fields who can contribute for the growth and prosperity of Bioinformatics/ cheminformatics / Biomedical informatics as a career .
BII is an initiative of Confrere Education Society. BII is the pioneer in the field of Bioinformatics and is today recognized across the globe as a premier institution offering programs in the area of Bioinformatics, Clinical Trials, Pharma Regulatory affairs, Pharma Quality Assurance and Control, Drug Design and Patenting, IPR and Biotechnology etc. We offer these training programs through various modes including distance participation, e-learning, classroom etc. We also conduct Workshops, Corporate trainings from time to time. Our quarterly journal Bioinformatics – Trends is one of its kind journal in India. We are also proud to supply multimedia and corporate training kits to governments, private bodies and individuals in our areas of expertise. BII is the biggest training organization in its field in India.Subject Areas of Specialsation
Bioinformatics
Pharma Regulatory Affairs
Clinical Trial Research and Administration
Intellectual Property Rights
Drug Design and Patenting
Biotechnology
Activities
Distance Participation Programs
Student Project & Trainings
Classroom Programs
Publications – Training Material, Books and Journals
Corporate Trainings
Multimedia and Video Based Corporate Training Kits
Workshops and Seminars Distance Participation Programs
Our Distance Participation Industry programs are our most popular programs. Working professionals from hundreds of reputed companies and students from elite institutes have participated and benefitted from these programs. BII is proud to have participants from more than 20 countries in these programs. The programs currently on offer are:
Industry Program in Bioinformatics
Industry Program in Pharma Regulatory Affairs
Industry Program in Clinical Trials, Research and Administration
Industry program in Pharma Quality Assurance and Quality Control
Industry program in Drug Design and patenting
Industry program in Intellectual Property Rights
Industry Program in Biotechnology
Introductory Program in Bioinformatics. Student Projects & Trainings
BII provides opportunity to students from various universities and colleges take up projects and trainings. We conduct two and six months projects in various domains such as Data Base Creation, Bioinformatics Tools, Computational Biology, Bioinformatics Software Development, Drug Designing, Phylogenetic Analysis, Data Mining, Molecular Biology. Structural and Functional Analysis of the sequences. Students may utilize these projects for submission at their respective institutes.Classroom Programs
BII offers classroom programs to a carefully chosen select group of students at Noida. The programs on offer are a 6 months , Advance Program in Boioinformatics for which admission is open two times a year. BII is also a local study center of Jamia Hamdard University and conducts its 12 month Post Graduate Diploma in Bioinformatics Program.
Publications – Training Material, Books and Journal
Our publications include a quarterly peer reviewed Journal “ Bioinformatics Trends”, A New Handbook of Bioinformatics, and training materials in areas like Bioinformatics, Clinical Trials, Pharma Regulatory Affairs, Drug Design and Discovery, Biotechnology etc. We have more than 30 publications to our credit. The“Bioinformatics Trends” journal publishes the high quality scientific papers and review articles of interest to academic and industrial researcher’s for keeping you update with the field of bioinformatics.
Corporate Trainings
BII offers training solutions designed specifically to meet the needs of our corporate clients. Our mission is to enable world-class companies increase productivity and performance through their people. We work with corporate to identify their individual and company wide training needs to deliver training programs that meet their needs. Our corporate clients include Stride Arcolab, Vimta labs, Nicholas Piramal, Computer Sciences Corporation, IARI, A.I Optics etc.
Multimedia and Video Based Training Kits
Our multimedia and video based training kits on Clinical Trials, Bioinformatics, Biological Databases and Genetic Engineering etc are very popular with life science college and departments. These training kits have also been utilized by private companies in India and abroad.
Workshops and Seminars
BII organizes workshops in its areas of expertise with an aim to enhance the skill domain of professionals, teachers and students. These workshops provide innovative knowledge of the subject. Some of the successful workshops organized in recent past are
Workshop on Cheminformatics and Drug Designing
Workshop on Genomics
Workshop on Bioinformatics and its emerging Dimensions
Workshop on Computational Biology
Workshop on Forensic Science
The institute aims not only educational and research initiative in this direction but also vouch for creating a talent pool of professionals from various fields who can contribute for the growth and prosperity of Bioinformatics/ cheminformatics / Biomedical informatics as a career .
BII is an initiative of Confrere Education Society. BII is the pioneer in the field of Bioinformatics and is today recognized across the globe as a premier institution offering programs in the area of Bioinformatics, Clinical Trials, Pharma Regulatory affairs, Pharma Quality Assurance and Control, Drug Design and Patenting, IPR and Biotechnology etc. We offer these training programs through various modes including distance participation, e-learning, classroom etc. We also conduct Workshops, Corporate trainings from time to time. Our quarterly journal Bioinformatics – Trends is one of its kind journal in India. We are also proud to supply multimedia and corporate training kits to governments, private bodies and individuals in our areas of expertise. BII is the biggest training organization in its field in India.Subject Areas of Specialsation
Bioinformatics
Pharma Regulatory Affairs
Clinical Trial Research and Administration
Intellectual Property Rights
Drug Design and Patenting
Biotechnology
Activities
Distance Participation Programs
Student Project & Trainings
Classroom Programs
Publications – Training Material, Books and Journals
Corporate Trainings
Multimedia and Video Based Corporate Training Kits
Workshops and Seminars Distance Participation Programs
Our Distance Participation Industry programs are our most popular programs. Working professionals from hundreds of reputed companies and students from elite institutes have participated and benefitted from these programs. BII is proud to have participants from more than 20 countries in these programs. The programs currently on offer are:
Industry Program in Bioinformatics
Industry Program in Pharma Regulatory Affairs
Industry Program in Clinical Trials, Research and Administration
Industry program in Pharma Quality Assurance and Quality Control
Industry program in Drug Design and patenting
Industry program in Intellectual Property Rights
Industry Program in Biotechnology
Introductory Program in Bioinformatics. Student Projects & Trainings
BII provides opportunity to students from various universities and colleges take up projects and trainings. We conduct two and six months projects in various domains such as Data Base Creation, Bioinformatics Tools, Computational Biology, Bioinformatics Software Development, Drug Designing, Phylogenetic Analysis, Data Mining, Molecular Biology. Structural and Functional Analysis of the sequences. Students may utilize these projects for submission at their respective institutes.Classroom Programs
BII offers classroom programs to a carefully chosen select group of students at Noida. The programs on offer are a 6 months , Advance Program in Boioinformatics for which admission is open two times a year. BII is also a local study center of Jamia Hamdard University and conducts its 12 month Post Graduate Diploma in Bioinformatics Program.
Publications – Training Material, Books and Journal
Our publications include a quarterly peer reviewed Journal “ Bioinformatics Trends”, A New Handbook of Bioinformatics, and training materials in areas like Bioinformatics, Clinical Trials, Pharma Regulatory Affairs, Drug Design and Discovery, Biotechnology etc. We have more than 30 publications to our credit. The“Bioinformatics Trends” journal publishes the high quality scientific papers and review articles of interest to academic and industrial researcher’s for keeping you update with the field of bioinformatics.
Corporate Trainings
BII offers training solutions designed specifically to meet the needs of our corporate clients. Our mission is to enable world-class companies increase productivity and performance through their people. We work with corporate to identify their individual and company wide training needs to deliver training programs that meet their needs. Our corporate clients include Stride Arcolab, Vimta labs, Nicholas Piramal, Computer Sciences Corporation, IARI, A.I Optics etc.
Multimedia and Video Based Training Kits
Our multimedia and video based training kits on Clinical Trials, Bioinformatics, Biological Databases and Genetic Engineering etc are very popular with life science college and departments. These training kits have also been utilized by private companies in India and abroad.
Workshops and Seminars
BII organizes workshops in its areas of expertise with an aim to enhance the skill domain of professionals, teachers and students. These workshops provide innovative knowledge of the subject. Some of the successful workshops organized in recent past are
Workshop on Cheminformatics and Drug Designing
Workshop on Genomics
Workshop on Bioinformatics and its emerging Dimensions
Workshop on Computational Biology
Workshop on Forensic Science
Job Opportunities at Reliance Clinical Research
Careers
Reliance Clinical Research Services (RCRS) is a full-service Contract Research Organization based in Mumbai, India. RCRS provides a broad range of clinical research services to assist pharmaceutical companies in bringing new products to the market. RCRS offers the domestic and international pharmaceutical, biotechnology and medical device companies, services at extremely competitive and affordable costs. We utilize the infrastructure of our parent company Reliance Industries Limited for the coordination of clinical trials activities; the benefits of the costs savings are passed on to our clients. RCRS has the advantage of offering the entire gamut of pre-clinical, clinical and post marketing services within the same comprehensive project management systems, thereby ensuring a smooth flow of data between paper and electronic reportoires with a high adherence to quality control. Each of our services are governed by rigorous Standard Operating Procedures and Policies which adhere to the more stringent of ICH-GCP and applicable regulatory guidelines.RCRS is proud of its role in helping sponsors achieve success in improving healthcare.We believe the following attributes define future Leadership in RCRS:
Customer centricity
Initiative and an attitude of ownership
Passion for excellence and ability to motivate team
Problem solving and an innovative "can do" mindset
Entrepreneurship and stretch
Today RCRS offers challenging assignments and career opportunities to candidates with expertise in the field of clinical research in the areas of Clinical Operations, Regulatory, Information Technology, Biometrics, Medical Affairs, Quality Assurance and Pharmacovigilance.
RCRS offers its employees a challenging career and performance based financial and other growth incentives and perks. The Human Resources department utilizes modern tools and innovative methods to assess the performance of each of its staff members thus making the growth process transparent. Employees of RCRS are part of a happy and satisfying environment. RCRS offers its employees cross functional roles which enhances their intellectual growth.
Please provide your resume so that as and when we find suitable opportunities we could contact you based on our review of your profile. We invite you to join us in creating an exciting future and to build a career in clinical research with the unique mission of "Bringing Research To Life".
visit www.relclin.com for details
Reliance Clinical Research Services (RCRS) is a full-service Contract Research Organization based in Mumbai, India. RCRS provides a broad range of clinical research services to assist pharmaceutical companies in bringing new products to the market. RCRS offers the domestic and international pharmaceutical, biotechnology and medical device companies, services at extremely competitive and affordable costs. We utilize the infrastructure of our parent company Reliance Industries Limited for the coordination of clinical trials activities; the benefits of the costs savings are passed on to our clients. RCRS has the advantage of offering the entire gamut of pre-clinical, clinical and post marketing services within the same comprehensive project management systems, thereby ensuring a smooth flow of data between paper and electronic reportoires with a high adherence to quality control. Each of our services are governed by rigorous Standard Operating Procedures and Policies which adhere to the more stringent of ICH-GCP and applicable regulatory guidelines.RCRS is proud of its role in helping sponsors achieve success in improving healthcare.We believe the following attributes define future Leadership in RCRS:
Customer centricity
Initiative and an attitude of ownership
Passion for excellence and ability to motivate team
Problem solving and an innovative "can do" mindset
Entrepreneurship and stretch
Today RCRS offers challenging assignments and career opportunities to candidates with expertise in the field of clinical research in the areas of Clinical Operations, Regulatory, Information Technology, Biometrics, Medical Affairs, Quality Assurance and Pharmacovigilance.
RCRS offers its employees a challenging career and performance based financial and other growth incentives and perks. The Human Resources department utilizes modern tools and innovative methods to assess the performance of each of its staff members thus making the growth process transparent. Employees of RCRS are part of a happy and satisfying environment. RCRS offers its employees cross functional roles which enhances their intellectual growth.
Please provide your resume so that as and when we find suitable opportunities we could contact you based on our review of your profile. We invite you to join us in creating an exciting future and to build a career in clinical research with the unique mission of "Bringing Research To Life".
visit www.relclin.com for details
Job Opportunities at Strides Arcolabs
Careers
At Strides, the truly global pharma company, each day is more exciting – you never know from which part of the world the challenge may come!
Work environmentThe work environment at Strides is full of excitement- we encourage creativity and innovation that go hand in hand with ownership. Development and growth is clearly road mapped with on going training programmes and workshops. We are also in the process of tying up with leading teaching institutes for professional job oriented courses. Apart from providing a fulfilling professional environment we also ensure competitive salaries.Current Openings:
1.
Manager - HR
2.
Warehouse Manager
3.
Manager - Legal
4.
Sr Executive /Executive - Regulatory Affairs Department RAD
5.
Group Leader - Safety, Health & Environment
6.
Sr. Executive / Executive - Strategic Sourcing
7.
Engineering Executive
8.
Team Leader - QMS & Documentation Assurance
9.
Executive/Sr.Executive - Analytical Services
10.
Executive/Sr.Executive - Technical Service Group (QA)
Benefits packageEmployee benefits include:- Competitive salary- Annual bonus- Leave travel allowance- Contributory provident fund
We welcome pharma professionals in the areas of R&D, Manufacturing, Regulatory Affairs, Quality Assurance and Analytical Services. Interested? Send your resume to: careers@stridesarco.com We assure you that your application will be kept in strict confidence.
VSS
At Strides, the truly global pharma company, each day is more exciting – you never know from which part of the world the challenge may come!
Work environmentThe work environment at Strides is full of excitement- we encourage creativity and innovation that go hand in hand with ownership. Development and growth is clearly road mapped with on going training programmes and workshops. We are also in the process of tying up with leading teaching institutes for professional job oriented courses. Apart from providing a fulfilling professional environment we also ensure competitive salaries.Current Openings:
1.
Manager - HR
2.
Warehouse Manager
3.
Manager - Legal
4.
Sr Executive /Executive - Regulatory Affairs Department RAD
5.
Group Leader - Safety, Health & Environment
6.
Sr. Executive / Executive - Strategic Sourcing
7.
Engineering Executive
8.
Team Leader - QMS & Documentation Assurance
9.
Executive/Sr.Executive - Analytical Services
10.
Executive/Sr.Executive - Technical Service Group (QA)
Benefits packageEmployee benefits include:- Competitive salary- Annual bonus- Leave travel allowance- Contributory provident fund
We welcome pharma professionals in the areas of R&D, Manufacturing, Regulatory Affairs, Quality Assurance and Analytical Services. Interested? Send your resume to: careers@stridesarco.com We assure you that your application will be kept in strict confidence.
VSS
Job Opportunities at Nicholas Piramal India Ltd
R & D Opportunities
Brief note on the divisionNPIL is engaged in major R&D initiatives in New Drug Discovery, Herbal Drugs, Chemical Process Development, Novel Drug Delivery System, Formulation Development and Clinical Research.To strengthen our R&D team, we are looking for committed, dynamic and ambitious R&D professionals with a proven track record and having flair for innovative research to take up challenging responsibilities in the following areas of expertise/specialization.
Desired AbilitiesCandidates for the positions mentioned below. should have the ability to lead a team of M.S. and Ph.D. level researchers. Experience in new drug discovery research would be an added advantage. Candidates must have the ability to effectively incorporate new scientific discoveries/ideas from various sources and have the ability/desire to operate in a team environment .The above positions require leadership and team building abilities with strong communication and personnel management skillsContactE-mail/ mail your CVs to researchrecruit@nicholaspiramal.co.in or to Nicholas Piramal India Limited, Nicholas Piramal Research Centre, 1-Nirlon Complex, Near NSE Complex, Off Western Express Highway, Goregaon (East), Mumbai 400 063, indicating the specialisation applied for.LocationNicholas Piramal Research Centre, Goregaon
Corporate Regulatory Affairs
Manager
Executive
Patents
Manager - In-house Patent attorney
Manager
Pharmaceutical R&D
Formulator
Analyst
Clinical Research Department
Executive
Analytical Science
Junior Research Scientist / Research Scientist
Corporate Regulatory Affairs
Manager
Educational Qualification : Bachelors or Masters in Pharmacy (B.Pharm/ M.Pharm) or a Bachelors or Masters in Science (B.Sc/M.Sc).
Experience : 5 years of experience essential; 6-7 years or more desirable. Knowledge of drug legislation, artwork, block proof approvals, filing State FDA applications, Central FDA applications, computer skills–MS Office, Corel Draw desirable. The candidate would be expected to co-ordinate with graphic artists for preparation of artwork, co-ordinate with various departments within the organization and manufacturing sites. Experience in preparation of application papers for obtaining various licenses and certificates essential.
The candidate should be willing to travel to various suppliers, artists’ premises, FDA offices, loan license locations, manufacturing sites, etc.
Corporate Regulatory Affairs
Executive
Educational Qualification : Bachelors or Masters in Pharmacy (BPharm/ MPharm) or a Bachelors or Masters in Science (B.Sc/M.Sc).
Experience : 2 years of experience essential; 3 years or more desirable. Knowledge of drug legislation, artwork, filing of FDA applications, computer skills–MS Office, Corel Draw desirable. The candidate would be expected to co-ordinate with graphic artists for preparation of artwork, co-ordinate with various departments within the organization and manufacturing sites. Experience in preparation of application papers for obtaining various licenses and certificates, analysis of packaging materials required.
The candidate should be willing to travel to various suppliers, and artists’ premises, etc.
Patents
Manager - In-house patent attorney
Patent personnel possessing a law degree with technical qualification in chemistry, biotechnology or pharmacy, having at least 3 years experience in patentability and infringement analysis, patent drafting and patent prosecution and other patent related aspects of pharmaceutical industries.
The candidate must have excellent analytical, reasoning and justification skills and a good understanding of patent laws of different countries, particularly India, USA and Europe.
Patents
Manager
Patent personnel, M.Sc/ Ph.D / M.Pharm, preferably with specialization in Biochemistry, Biotechnology or Molecular Biology, with at least two years experience in carrying out prior art searches, rendering well-reasoned opinions on matters of patentability, freedom to operate and patent infringement, drafting and filing patent applications, and patent prosecution, especially for biological inventions. A degree in Law or postgraduate diploma in patent law will be an added advantage.
The candidate must have excellent analytical and writing skills.
Pharmaceutical R&D
Formulator
Age group : 25 to 32 yearsQualifications : Minimum qualifications required B.Pharm, Preferred an M.Pharm/ PhDExperience : 1 to 5 yearsJob Description : The person will be responsible for carrying out laboratory trials, scale up trials and technology transfer of a product. He/ she will be required to prepare documents required for technology transfer to Plant. Formulation : Design, development, manufacturing process development and technology transfer. Prior experience in ANDA preferred; Knowledge of regulatory requirements. If the candidate possesses Novel Drug Delivery System experience, then NDDS 'ANDA' preferred.
Good communication and documentation skills are a must. Computer literacy and exposure to GLP philosophy desired.
Pharmaceutical R&D
AnalystAge group : 25 to 32 yearsQualifications : Minimum qualifications required M.Sc/M.Pharm, Preferred a Ph.D.Experience : 1 to 5 yearsRequirements : Experience in analytical method development for finished dosage forms is a must Experience in handling HPLC with latest software required. Experience in dissolution method development is a must. Knowledge of impurity profiling and method validation desirable.
Good communication and documentation skills are a must. Computer literacy and exposure to GLP philosophy desired.
Clinical Research Department
ExecutiveEducational Qualification : Bachelors or Masters in Pharmacy (BPharm/ MPharm) or a Bachelors or Masters in Science (B.Sc/M.Sc) in a biological or science related field essential.
Experience : 6 months -1 year hands-on experience of monitoring Clinical Trials ( Phase II to IV Clinical Trials preferred). Knowledge of procedures for monitoring clinical trials, GCP, etc, desired. Good verbal and written communications skills desired along with knowledge of management of clinical studies. Ability to work independently, as well as part of a project team. Computer literacy is a must. The candidate should be willing to travel.
Analytical Science
Junior Research Scientist/ Research ScientistQualifications and Other Required Knowledge and Skills: Masters (M.Sc) in Analytical Chemistry / Chemistry / Applied Chemistry with 3 to 4 years of experience or Ph.D degree in analytical chemistry or a related field with relevant analytical experience in small molecule analysis. Expertise in HPLC/MS and detector technology (such as UV, ELSD, RI or MS detectors), in modern data acquisition and in handling software is essential. Hands-on experience with HPLC systems as well as familiarity with GMP (or equivalent) analytical documentation are required. Prior experience in formulation analysis or drug product stability testing in a GMP setting is preferred. Qualified candidates must be able to work independently and have excellent organizational, communication and problem solving abilities.
Responsibilities: To analyze, process, and evaluate data generated from biological samples processed in the Bioanalytical Laboratory and support submissions to regulatory agencies. To develop quantitative LC and LC/MS/MS based bioanalytical methods, method validation, documentation as per GLP norms and generate data as per ICH / US FDA guidelines. To carry out periodical calibration, standardization of instruments with complete documentation and update SOPs as and when required. To calibrate stability chambers and maintain IQ, OQ and PQ of all the facilities used for bio-analysis as per GLP norms. To participate in other analytical activities, such as impurity identification, reference marker preparation, solubility and stability determination, analytical documentation preparation, as well as method transfer, internally or externally. Knowledge of FDA GLPs and chromatographic techniques is required.
Brief note on the divisionNPIL is engaged in major R&D initiatives in New Drug Discovery, Herbal Drugs, Chemical Process Development, Novel Drug Delivery System, Formulation Development and Clinical Research.To strengthen our R&D team, we are looking for committed, dynamic and ambitious R&D professionals with a proven track record and having flair for innovative research to take up challenging responsibilities in the following areas of expertise/specialization.
Desired AbilitiesCandidates for the positions mentioned below. should have the ability to lead a team of M.S. and Ph.D. level researchers. Experience in new drug discovery research would be an added advantage. Candidates must have the ability to effectively incorporate new scientific discoveries/ideas from various sources and have the ability/desire to operate in a team environment .The above positions require leadership and team building abilities with strong communication and personnel management skillsContactE-mail/ mail your CVs to researchrecruit@nicholaspiramal.co.in or to Nicholas Piramal India Limited, Nicholas Piramal Research Centre, 1-Nirlon Complex, Near NSE Complex, Off Western Express Highway, Goregaon (East), Mumbai 400 063, indicating the specialisation applied for.LocationNicholas Piramal Research Centre, Goregaon
Corporate Regulatory Affairs
Manager
Executive
Patents
Manager - In-house Patent attorney
Manager
Pharmaceutical R&D
Formulator
Analyst
Clinical Research Department
Executive
Analytical Science
Junior Research Scientist / Research Scientist
Corporate Regulatory Affairs
Manager
Educational Qualification : Bachelors or Masters in Pharmacy (B.Pharm/ M.Pharm) or a Bachelors or Masters in Science (B.Sc/M.Sc).
Experience : 5 years of experience essential; 6-7 years or more desirable. Knowledge of drug legislation, artwork, block proof approvals, filing State FDA applications, Central FDA applications, computer skills–MS Office, Corel Draw desirable. The candidate would be expected to co-ordinate with graphic artists for preparation of artwork, co-ordinate with various departments within the organization and manufacturing sites. Experience in preparation of application papers for obtaining various licenses and certificates essential.
The candidate should be willing to travel to various suppliers, artists’ premises, FDA offices, loan license locations, manufacturing sites, etc.
Corporate Regulatory Affairs
Executive
Educational Qualification : Bachelors or Masters in Pharmacy (BPharm/ MPharm) or a Bachelors or Masters in Science (B.Sc/M.Sc).
Experience : 2 years of experience essential; 3 years or more desirable. Knowledge of drug legislation, artwork, filing of FDA applications, computer skills–MS Office, Corel Draw desirable. The candidate would be expected to co-ordinate with graphic artists for preparation of artwork, co-ordinate with various departments within the organization and manufacturing sites. Experience in preparation of application papers for obtaining various licenses and certificates, analysis of packaging materials required.
The candidate should be willing to travel to various suppliers, and artists’ premises, etc.
Patents
Manager - In-house patent attorney
Patent personnel possessing a law degree with technical qualification in chemistry, biotechnology or pharmacy, having at least 3 years experience in patentability and infringement analysis, patent drafting and patent prosecution and other patent related aspects of pharmaceutical industries.
The candidate must have excellent analytical, reasoning and justification skills and a good understanding of patent laws of different countries, particularly India, USA and Europe.
Patents
Manager
Patent personnel, M.Sc/ Ph.D / M.Pharm, preferably with specialization in Biochemistry, Biotechnology or Molecular Biology, with at least two years experience in carrying out prior art searches, rendering well-reasoned opinions on matters of patentability, freedom to operate and patent infringement, drafting and filing patent applications, and patent prosecution, especially for biological inventions. A degree in Law or postgraduate diploma in patent law will be an added advantage.
The candidate must have excellent analytical and writing skills.
Pharmaceutical R&D
Formulator
Age group : 25 to 32 yearsQualifications : Minimum qualifications required B.Pharm, Preferred an M.Pharm/ PhDExperience : 1 to 5 yearsJob Description : The person will be responsible for carrying out laboratory trials, scale up trials and technology transfer of a product. He/ she will be required to prepare documents required for technology transfer to Plant. Formulation : Design, development, manufacturing process development and technology transfer. Prior experience in ANDA preferred; Knowledge of regulatory requirements. If the candidate possesses Novel Drug Delivery System experience, then NDDS 'ANDA' preferred.
Good communication and documentation skills are a must. Computer literacy and exposure to GLP philosophy desired.
Pharmaceutical R&D
AnalystAge group : 25 to 32 yearsQualifications : Minimum qualifications required M.Sc/M.Pharm, Preferred a Ph.D.Experience : 1 to 5 yearsRequirements : Experience in analytical method development for finished dosage forms is a must Experience in handling HPLC with latest software required. Experience in dissolution method development is a must. Knowledge of impurity profiling and method validation desirable.
Good communication and documentation skills are a must. Computer literacy and exposure to GLP philosophy desired.
Clinical Research Department
ExecutiveEducational Qualification : Bachelors or Masters in Pharmacy (BPharm/ MPharm) or a Bachelors or Masters in Science (B.Sc/M.Sc) in a biological or science related field essential.
Experience : 6 months -1 year hands-on experience of monitoring Clinical Trials ( Phase II to IV Clinical Trials preferred). Knowledge of procedures for monitoring clinical trials, GCP, etc, desired. Good verbal and written communications skills desired along with knowledge of management of clinical studies. Ability to work independently, as well as part of a project team. Computer literacy is a must. The candidate should be willing to travel.
Analytical Science
Junior Research Scientist/ Research ScientistQualifications and Other Required Knowledge and Skills: Masters (M.Sc) in Analytical Chemistry / Chemistry / Applied Chemistry with 3 to 4 years of experience or Ph.D degree in analytical chemistry or a related field with relevant analytical experience in small molecule analysis. Expertise in HPLC/MS and detector technology (such as UV, ELSD, RI or MS detectors), in modern data acquisition and in handling software is essential. Hands-on experience with HPLC systems as well as familiarity with GMP (or equivalent) analytical documentation are required. Prior experience in formulation analysis or drug product stability testing in a GMP setting is preferred. Qualified candidates must be able to work independently and have excellent organizational, communication and problem solving abilities.
Responsibilities: To analyze, process, and evaluate data generated from biological samples processed in the Bioanalytical Laboratory and support submissions to regulatory agencies. To develop quantitative LC and LC/MS/MS based bioanalytical methods, method validation, documentation as per GLP norms and generate data as per ICH / US FDA guidelines. To carry out periodical calibration, standardization of instruments with complete documentation and update SOPs as and when required. To calibrate stability chambers and maintain IQ, OQ and PQ of all the facilities used for bio-analysis as per GLP norms. To participate in other analytical activities, such as impurity identification, reference marker preparation, solubility and stability determination, analytical documentation preparation, as well as method transfer, internally or externally. Knowledge of FDA GLPs and chromatographic techniques is required.
Tuesday, November 13, 2007
Pharma Regulatory Affairs Career Centre
Bioinformatics Institute of India, BII has been a pioneering institution in running Pharma Regulatory Affairs Programs. So far professionals from several hundred reputed phama companies have joined BII programs
The popularity of BII Pharma Regulatory Program has been mainly due to the following reasons
1) Proven training methodology involving recorded lectures, training material (printed books, assignments research study etc) e-learning etc for Pharma Regulatory Affairs
2) Continuous demand for Pharma Regulatory Professionals in India and abroad.
3) Excellent industry interface of the Institute
4) Corporate Nominations from numerous pharma companies like Vimta Labs, Nicholas Piramal, Stride Arcolabs etc
5) Rapid placement and career progression of BII Pharma Regulatory students
Today the demand for Pharma Regulatory Affairs students from BII is like never before. To enhance and accelerate this process BII has established Pharma Regulatory Affairs Career Centre for its program participants. All the program participants will be provided following support
1) Sending of Resume to Pharma Regulatory Departments of Companies and to Pharma Regulatory Affairs Consultants
2) Resume Making and Interview tips
3) Information about Companies and Jobs in the Pharma Regulatory Affairs Area
For Further details about, Pharma Regulatory Affairs Career Centre
Contact BII Support at 9810535368 and 9818473366
for BII
The popularity of BII Pharma Regulatory Program has been mainly due to the following reasons
1) Proven training methodology involving recorded lectures, training material (printed books, assignments research study etc) e-learning etc for Pharma Regulatory Affairs
2) Continuous demand for Pharma Regulatory Professionals in India and abroad.
3) Excellent industry interface of the Institute
4) Corporate Nominations from numerous pharma companies like Vimta Labs, Nicholas Piramal, Stride Arcolabs etc
5) Rapid placement and career progression of BII Pharma Regulatory students
Today the demand for Pharma Regulatory Affairs students from BII is like never before. To enhance and accelerate this process BII has established Pharma Regulatory Affairs Career Centre for its program participants. All the program participants will be provided following support
1) Sending of Resume to Pharma Regulatory Departments of Companies and to Pharma Regulatory Affairs Consultants
2) Resume Making and Interview tips
3) Information about Companies and Jobs in the Pharma Regulatory Affairs Area
For Further details about, Pharma Regulatory Affairs Career Centre
Contact BII Support at 9810535368 and 9818473366
for BII
Career Assistance for BII Industry Programs
Following Career Assistance is provided to BII Industry Program Participants
Students are provided with a resume writing guideline.
All students have their resume evaluated by experienced BII Professionals.
Successful graduates have their resume distributed to several hundred potential employers (Bioinformatics, pharmaceutical companies, contract research organizations, academic institutions, and research sites).
The student’s resume will also be placed on this blog along with job postings which we receive.
Resumes will be posted on this blog for free access by employers.
Please note: Industry sponsored students are not eligible for career assistance.
BII alumni is today present in hundreds of Pharma, IT, Biotech and consultancy companies we constantly reach out to our alumni for placement activities
for BII
Students are provided with a resume writing guideline.
All students have their resume evaluated by experienced BII Professionals.
Successful graduates have their resume distributed to several hundred potential employers (Bioinformatics, pharmaceutical companies, contract research organizations, academic institutions, and research sites).
The student’s resume will also be placed on this blog along with job postings which we receive.
Resumes will be posted on this blog for free access by employers.
Please note: Industry sponsored students are not eligible for career assistance.
BII alumni is today present in hundreds of Pharma, IT, Biotech and consultancy companies we constantly reach out to our alumni for placement activities
for BII
Change in Address of Calcutta Centre - November 24 and 25 Exams
Dear Participants ( All those appearing at Kolkatta Centre for November 24 and 25 exams)
Please note the change , the new address of Kolkata centre is as follows
INDIAN INSTITUTE OF PROFESSIONALS,14, Congress Exibhition Road,
Near Popsia Police Station, Kolkata, West Bengal, India - 700017
thanks
for BII Admin
Please note the change , the new address of Kolkata centre is as follows
INDIAN INSTITUTE OF PROFESSIONALS,14, Congress Exibhition Road,
Near Popsia Police Station, Kolkata, West Bengal, India - 700017
thanks
for BII Admin
Monday, November 12, 2007
Clinical Trial Companies
Dear Friends
In this ongoing post we will maintain a list of Clinical Trial companies with their websites
Accutest Research Laboratories http://www.accutestindia.com/
Dr Sahoos Clinical Services Pvt Ltd http://www.drsahoo.com/
Bio-Scientific Research Laboratories (I) Pvt Ltd email: biosrl@vsnl.net
Accutest Research Laboratories (I) Pvt. Ltd.
Ace Biomed Pvt. Ltd.
Adroit Insights Lifesciences Pvt. Ltd.
Apothecaries Ltd.
Asian Clinical Trials Pvt. Ltd.
Catalyst Clinical Services Pvt. Ltd.
Clinigene International Pvt. Ltd.
ClinInvent Research Pvt. Ltd.
ClinTec International Ltd.
Clintrac International Pvt. Ltd.
ClinWorld Pvt. Ltd.
Covance Inc.
Diagno-search (taken over by iGATE)
ICON Plc
iGATE Clinical Research International Pvt. Ltd.
Jubilant Clinsys Ltd.
Kendle International Inc.
Lambda Therapeutic Research Ltd.
Lotus Labs Pvt. Ltd.
Manipal Acunova Ltd.
Materiamedica Services Pvt. Ltd.
Neeman Medical International
Omnicare Clinical Research
Parexel International
Pharmaceutical Product Development, Inc.
Pharmanet Development Group, Inc.
Quintiles Spectral Ltd.
Reliance Clinical Research Services Pvt. Ltd.
Sipra Labs Pvt. Ltd.
SIRO Clinpharm Pvt. Ltd.
Suven Life Sciences Ltd.
Synchron Research Services Pvt. Ltd.
Vibgyor Care http://www.vibgyorcare.com/
Veeda Clinical Research Ltd.
Vimta Labs Ltd.
Wellquest International (India)
The above list will be updated on a periodic basis. For a detailed list you can obtain BII's free clinical trial directory be sending us an email at members@bioinformaticscentre.org
For BII's Clinical Trial Program you can visit www.bii.in/biodlp
For BII Admin
In this ongoing post we will maintain a list of Clinical Trial companies with their websites
Accutest Research Laboratories http://www.accutestindia.com/
Dr Sahoos Clinical Services Pvt Ltd http://www.drsahoo.com/
Bio-Scientific Research Laboratories (I) Pvt Ltd email: biosrl@vsnl.net
Accutest Research Laboratories (I) Pvt. Ltd.
Ace Biomed Pvt. Ltd.
Adroit Insights Lifesciences Pvt. Ltd.
Apothecaries Ltd.
Asian Clinical Trials Pvt. Ltd.
Catalyst Clinical Services Pvt. Ltd.
Clinigene International Pvt. Ltd.
ClinInvent Research Pvt. Ltd.
ClinTec International Ltd.
Clintrac International Pvt. Ltd.
ClinWorld Pvt. Ltd.
Covance Inc.
Diagno-search (taken over by iGATE)
ICON Plc
iGATE Clinical Research International Pvt. Ltd.
Jubilant Clinsys Ltd.
Kendle International Inc.
Lambda Therapeutic Research Ltd.
Lotus Labs Pvt. Ltd.
Manipal Acunova Ltd.
Materiamedica Services Pvt. Ltd.
Neeman Medical International
Omnicare Clinical Research
Parexel International
Pharmaceutical Product Development, Inc.
Pharmanet Development Group, Inc.
Quintiles Spectral Ltd.
Reliance Clinical Research Services Pvt. Ltd.
Sipra Labs Pvt. Ltd.
SIRO Clinpharm Pvt. Ltd.
Suven Life Sciences Ltd.
Synchron Research Services Pvt. Ltd.
Vibgyor Care http://www.vibgyorcare.com/
Veeda Clinical Research Ltd.
Vimta Labs Ltd.
Wellquest International (India)
The above list will be updated on a periodic basis. For a detailed list you can obtain BII's free clinical trial directory be sending us an email at members@bioinformaticscentre.org
For BII's Clinical Trial Program you can visit www.bii.in/biodlp
For BII Admin
Pharma Events Calendar
Dear All
In this post we wish to maintain the Pharma Events calendar for India and abroad we will cover pharma conferences , exhibitions and Programs in this
2007, November 1-3, Mumbai
Pharma Expo
2007, November 20 - 21, Mumbai
IN-COSMETICS India, The leading conference exhibition in India for Personal Care and Home Care Ingredients.
www.in-cosmeticsindia.com
2007, November 25 - 27, Mumbai, Bombay Exhibition Centre
CPhi India 2007
2007, November 28 - December 1, 2007, Miami Beach Florida
10th annual IGPA conference
Weblink: www.gphaonline.org
2007, December 20 - 23, Banaras
59th Indian Pharma Congress and Expo
Weblink: http://www.59thipcvaranasi.com/
2008, 28th - 31st January Dubai, UAE
Arab Health 2008
www.comnetexhibitions.com
2008 January 29 - February 1 New Orleans LA
informEx 2008 USA
www.informexusa.com
2008, February 16th-17th Kathmandu Nepal
Nepal Pharma Expo
www.appon.org
for BII
In this post we wish to maintain the Pharma Events calendar for India and abroad we will cover pharma conferences , exhibitions and Programs in this
2007, November 1-3, Mumbai
Pharma Expo
2007, November 20 - 21, Mumbai
IN-COSMETICS India, The leading conference exhibition in India for Personal Care and Home Care Ingredients.
www.in-cosmeticsindia.com
2007, November 25 - 27, Mumbai, Bombay Exhibition Centre
CPhi India 2007
2007, November 28 - December 1, 2007, Miami Beach Florida
10th annual IGPA conference
Weblink: www.gphaonline.org
2007, December 20 - 23, Banaras
59th Indian Pharma Congress and Expo
Weblink: http://www.59thipcvaranasi.com/
2008, 28th - 31st January Dubai, UAE
Arab Health 2008
www.comnetexhibitions.com
2008 January 29 - February 1 New Orleans LA
informEx 2008 USA
www.informexusa.com
2008, February 16th-17th Kathmandu Nepal
Nepal Pharma Expo
www.appon.org
for BII
PhD Enrollment at Centre for Cellular and Molecular Biology
Admissions to the PhD program are announced for CCMB. Advertisement has come up in the Times of India 12th of November. For details visit www.ccmb.res.in
For
BII
For
BII
Saturday, November 10, 2007
Reregistration for Autumn 06 Batch
Dear Participants of Autumn 06 Batch
All those who are not appearing in November 2007 examinations have to reregister for the next session. Reregistration details can be obtained at info@bioinformaticscentre.org or at BII Support. Reregistered candidates can appear in April 2008 and November 2008 exams.
BII Support numbers are 0120-43201801 and 4310802, Mobile Numbers are 9810535368 and 9818473366
thanks
BII Admin
All those who are not appearing in November 2007 examinations have to reregister for the next session. Reregistration details can be obtained at info@bioinformaticscentre.org or at BII Support. Reregistered candidates can appear in April 2008 and November 2008 exams.
BII Support numbers are 0120-43201801 and 4310802, Mobile Numbers are 9810535368 and 9818473366
thanks
BII Admin
IT Companies Bet Big on the Bioinformatics Domain
Dear Friends
As is known to all all the big IT companies in India like TCS, Infosys, Wipro, Satyam, Accenture, IBM, HCL etc have made significant investments in their lifescience IT offerings. These include services in
Drug Discovery and Research
Bioinformatics
Clinical Trials
Biotechnology
These companies offer IT products and services to their clients in Pharma, Biotech, Agri and Hospital sectors. We are providing links of some of the industry reports for you to get an idea of whats up
Satyam Forays into Bioinformatics http://in.news.yahoo.com/071028/48/6mist.html
Latest Bioinformatics IT company Report
http://www.thehindubusinessline.com/2007/06/09/stories/2007060905791000.htm
TCS into Bioinformatics
http://www.tata.com/tcs/articles/20070625_innovation_labs.htm
Bioinformatics Industry Report
http://biospectrumindia.ciol.com/content/careers/10306091.asp
Infosys Foray into Biotechnology
http://www.financialexpress.com/news/story/101482/
CDAC Bioinformatics Industry Report
http://www.cdac.in/html/press/3q03/spot357.asp
Clinical Trial White Papers
http://www.bii.in/pharma/cr_ci_new_prospectus.asp
With Thanks
from BII Admin
As is known to all all the big IT companies in India like TCS, Infosys, Wipro, Satyam, Accenture, IBM, HCL etc have made significant investments in their lifescience IT offerings. These include services in
Drug Discovery and Research
Bioinformatics
Clinical Trials
Biotechnology
These companies offer IT products and services to their clients in Pharma, Biotech, Agri and Hospital sectors. We are providing links of some of the industry reports for you to get an idea of whats up
Satyam Forays into Bioinformatics http://in.news.yahoo.com/071028/48/6mist.html
Latest Bioinformatics IT company Report
http://www.thehindubusinessline.com/2007/06/09/stories/2007060905791000.htm
TCS into Bioinformatics
http://www.tata.com/tcs/articles/20070625_innovation_labs.htm
Bioinformatics Industry Report
http://biospectrumindia.ciol.com/content/careers/10306091.asp
Infosys Foray into Biotechnology
http://www.financialexpress.com/news/story/101482/
CDAC Bioinformatics Industry Report
http://www.cdac.in/html/press/3q03/spot357.asp
Clinical Trial White Papers
http://www.bii.in/pharma/cr_ci_new_prospectus.asp
With Thanks
from BII Admin
BII Programs
Your Institute BII has been proud to offer its programs in Bioinformatics, Biotechnology, IPR and
Pharma (Regulatory Affairs, Clinical Trials, GMP, Drug Design and Patenting) domains. BII since
its inception in 2002 has been a pioneering and a leading institution. So far BII has been able to reach more than 10,000 participants through its distance participation, classroom and project programs. The course content, electronic lectures and other activities like placement support have benifitted participants from hundreds of leading Pharma, Biotech, IT, Agri an consultancy companies. BII programs have accelerated and enhanced careers and knowledge.Program. We have significantly increased our industry interaction and are constantly forwarding resumes of our participants to the industry. Admissions to the Autmn 2007 session are open and working professionals and highly motivated students are welcome to join them.
Details www.bii.in/biodlp
Thanks
For BII Admin
Pharma (Regulatory Affairs, Clinical Trials, GMP, Drug Design and Patenting) domains. BII since
its inception in 2002 has been a pioneering and a leading institution. So far BII has been able to reach more than 10,000 participants through its distance participation, classroom and project programs. The course content, electronic lectures and other activities like placement support have benifitted participants from hundreds of leading Pharma, Biotech, IT, Agri an consultancy companies. BII programs have accelerated and enhanced careers and knowledge.Program. We have significantly increased our industry interaction and are constantly forwarding resumes of our participants to the industry. Admissions to the Autmn 2007 session are open and working professionals and highly motivated students are welcome to join them.
Details www.bii.in/biodlp
Thanks
For BII Admin
Thursday, November 8, 2007
6 Months Pharma GMP Program
Dear All
This is to verify that the Institute has introduced a 6 Months Pharma GMP Program. This has been started after receiving good demand from pharma industry and individual applicants
thanks
BII Admin
This is to verify that the Institute has introduced a 6 Months Pharma GMP Program. This has been started after receiving good demand from pharma industry and individual applicants
thanks
BII Admin
Tuesday, November 6, 2007
Lectures on Mobile Phones
Dear All
Institute is happy to announce that following lectures of the duration 45 minutes to 1 hour are being prepared by the Institute. These lectures can be run on mobile phones and Personal computers. As soon as the lectures are ready they will be made available through this blog
Topics are
1) Regulatory Affairs Profession
2) Standard Operating Procedures
3) Pharmacovigilance
4) Clinical Data Managemenet
5) Bioinformatics Applications in the Industry
6) Clinical Trial Software
7) Role of IP Management in Drug Discovery Process
8) Clinical Trial Registry
9) Clinical Trial Forms
10) GMP in India
11) 21 CFR Regulations
Watch out this blog for further developments on this
For BII
Institute is happy to announce that following lectures of the duration 45 minutes to 1 hour are being prepared by the Institute. These lectures can be run on mobile phones and Personal computers. As soon as the lectures are ready they will be made available through this blog
Topics are
1) Regulatory Affairs Profession
2) Standard Operating Procedures
3) Pharmacovigilance
4) Clinical Data Managemenet
5) Bioinformatics Applications in the Industry
6) Clinical Trial Software
7) Role of IP Management in Drug Discovery Process
8) Clinical Trial Registry
9) Clinical Trial Forms
10) GMP in India
11) 21 CFR Regulations
Watch out this blog for further developments on this
For BII
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