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Clarivate looking for Pharmacovigilance Manager - M.Pharm, MSc Apply

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Clarivate looking for Pharmacovigilance Manager

Clarivate is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world's most complex problems by providing actionable information and insights that reduce the time from new ideas to life-changing inventions in the areas of     science and intellectual property. We help customers discover, protect and commercialize their inventions using our trusted subscription and technology-based solutions coupled with deep domain expertise.

Post : Manager, Pharmacovigilance

Job Description
The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.

• Certification from a professional medical writer’s association
• Experience with commercial and client-specific biomedical literature databases
• Scientific/medical writing background
• Providing functional expertise/oversight of process and handling queries of the PV Operations staff
• Create
• Participation in meetings with client and within team, as needed.
• Performing activities delegated to the PV Operations staff in case of unplanned peaks or urgent requirements
• Prepare for and respond to internal/external audits/inspections
• Taking suitable action as per client feedback for any performance or process related concerns
• Providing project updates to the Senior Management on periodic basis
• Assisting his/her manager for operational day-to-day activities


Candidate Profile
• Master’s Degree in life Sciences, Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).
• A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantage
• Around 10 years of experience reviewing biomedical literature for adverse event reporting and atleast 5 years of team management experience
• Excellent leadership and line management skills
• Excellent knowledge of drug safety and the drug development process
• Client focused approach to work
• Ability to manage multiple and varied tasks and prioritize workload with attention to detail
• Ability to train and mentor people

Additional Information
Experience : 5+ years 
Qualification : M.Pharm / M.Sc
Location : Karnataka, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Life Sciences & Healthcare
End Date : 30th March 2025


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