Location: Hyderabad / Secunderabad
Compensation: Best in the Industry
Education:UG - B.Pharma - Pharmacy,B.Sc - Any Specialization, MBBS - Medicine
PG - Any PG Course - Any Specialization
Industry Type:Pharma/ Biotech/Clinical Research
Functional Area:Healthcare, Medical, R&D
Job Description
Responsibilities:
Processing, review and distributing expedited adverse event reports as appropriate in accordance with quality standards.
To respond and record all details of Medical Information queries in an accurate and consistent manner.
Be responsible for providing medical evaluation for case assessments and ensure correct assignment of seriousness for cases received within the company
To prepare Periodic Safety Update Reports, Bridging Summaries and Cumulative ADR Summaries.
To review the worldwide literature for suspected ADRs upon request.
To assist in the training of appropriate personnel in the relevant aspects of Pharmacovigilance
Assist Manager in special projects undertaken from time to time to ensure objectives and deadlines can be met
General filing, photocopying, scanning, etc for the Pharmacovigilance team, as required.
Assisting with any other Pharmacovigilance/Medical Information team projects as necessary.
MBBS, MD, MS,M.Pharm with pharmacovigilance experience.
Company Profile MedHimalayas is a technologically advanced, contract research organization specialize in Pharmacovigilance.
Contact Details
Company Name:MedHimalayas
Website:http://www.medhimalayas.com
Email Address:hr@medhimalayas.com
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