Pharmacovigilance Specialist Job at Clarivate- Life Sciences Apply Now!
Clarivate, a global leader in Life Sciences and Healthcare analytics, is hiring a Pharmacovigilance Specialist in Karnataka, India. This hybrid role involves analyzing biomedical literature, reporting adverse events, and ensuring drug safety compliance. Candidates with a Master’s in Life Sciences, Health, or Biomedical Sciences and experience in pharmacovigilance regulations are encouraged to apply. Apply now and be part of an innovative team shaping the future of drug safety!
Job Title: Pharmacovigilance Specialist
Location: Karnataka, India
Industry: Life Sciences & Healthcare
Remote: Hybrid
Job ID: JREQ131112
About You
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences
- Experience in reviewing biomedical literature for adverse event reporting
- Strong analytic ability and knowledge of pharmacovigilance regulations
Desired Qualifications
- Experience in drug safety/pharmacovigilance
- Proficiency in scientific/medical writing
- Certification from a professional medical writer’s association
Responsibilities
- Analyze articles from biomedical literature and internal drug safety alerts
- Write brief narratives summarizing safety relevant information
- Complete drug safety reviewing in accordance with regulatory requirements
About the Team
The PV Literature team at Clarivate supports multiple customers across various therapeutic areas. We offer a supportive working environment with personalized training and opportunities for professional growth.
Hours of Work
This is a full-time permanent position working weekdays (Monday to Friday), 11 am – 8 PM IST.
At Clarivate, we uphold equal employment opportunities and comply with non-discrimination laws and regulations.
Keywords: Pharmacovigilance Specialist, Life Sciences, Healthcare, Karnataka, Job Opening, Drug Safety, Medical Writing, Pharmacovigilance Specialist at Clarivate- Life Sciences Apply Now!
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