Pharmacovigilance Specialist / Lead PV Specialist
Location: Noida, Uttar Pradesh, India
Remote: Hybrid
Job ID: JREQ128594
Industry: Life Sciences & Healthcare
Job Overview
We are seeking a Pharmacovigilance Specialist / Lead PV Specialist to join our Pharmacovigilance (PV) team. This is a hybrid role where you will work both remotely and on-site. You will play a critical role in supporting our team by performing literature monitoring, assessing adverse events reporting, and using your extensive knowledge of scientific terms, medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
Responsibilities
- Analyze large volumes of biomedical literature and internal drug safety alerts.
- Identify individual case safety reports (ICSRs) and other safety-relevant information.
- Write concise summaries of ICSR criteria and safety-relevant information.
- Understand and apply client’s drug labels during safety assessments.
- Complete drug safety reviews accurately and timely.
- Use a drug safety system to track actions and assessments.
- Select and abstract relevant articles for the client’s product literature database.
- Maintain awareness of new drugs, therapeutic categories, and changes in biomedical terminology.
Required Qualifications
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics).
- Degree in Dentistry, Physiotherapy, or Nursing is a plus.
- At least 4 years of experience reviewing biomedical literature for adverse event reporting.
- Alternatively, 6 years of relevant experience with an information science degree.
- Strong analytical skills and ability to summarize biomedical case reports and studies.
- Proficient in biomedical terminology, drugs, and therapeutic areas.
- Experience in database/literature searches.
- Excellent interpersonal, verbal, and written communication skills.
- Ability to work collaboratively, manage tasks, and prioritize workload.
Preferred Qualifications
- Certification from a professional medical writer’s association.
- Experience with commercial and client-specific biomedical literature databases.
- Background in scientific/medical writing.
What We Offer
- A supportive work environment with personalized training.
- Opportunities to engage in various aspects of pharmacovigilance.
- Participation in customer upgrade planning if desired.
Hours of Work
- Full-time, permanent position.
- Weekdays (Monday to Friday).
Equal Employment Opportunity
At Clarivate, we are committed to equal employment opportunities. We ensure fairness in hiring, compensation, promotion, and all other employment terms in compliance with applicable laws and regulations.
