Pharmacovigilance Openings at Clarivate (multiple Locations)

Are you passionate about drug safety and pharmacovigilance? Clarivate is hiring an Associate Pharmacovigilance Specialist for its Bangalore and Noida offices in hybrid mode. This role offers the chance to work on biomedical literature monitoring, adverse event reporting, indexing, and scientific writing, contributing to patient safety worldwide.

If you have a strong background in life sciences, pharmacy, or biomedical sciences, this could be your next career step in the growing field of pharmacovigilance.

🔹 Key Responsibilities

As an Associate Pharmacovigilance Specialist, your role will include:

• Monitoring biomedical literature to identify adverse events.
• Abstracting, indexing, and summarizing scientific case reports and studies.
• Applying knowledge of pharmacovigilance regulations, medical terminology, and therapeutic areas.
• Preparing clear, concise, and accurate scientific summaries.
• Using commercial and client-specific biomedical literature databases.
• Working independently and collaboratively to meet client needs.

🎓 Qualifications & Skills

Required:

• Master’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Biophysics, or related fields.
• 1–2 years of experience in biomedical literature review for adverse events or equivalent background.
• Strong analytical and medical writing skills.
• Excellent command of English (reading, writing, comprehension, speaking).
• Familiarity with biomedical terminology, drug safety databases, and therapeutic areas.

Preferred:

• Certification from a professional medical writing association.
• Previous pharmacovigilance or drug safety experience.
• Background in scientific/medical writing.

💼 Benefits of Joining Clarivate

• Hybrid work model (Monday to Friday).
• Exposure to global drug safety and pharmacovigilance practices.
• Professional development opportunities.
• Inclusive, collaborative workplace culture.

📌 How to Apply

Application Link