Are you a life sciences professional looking to advance your career in pharmacovigilance? Clarivate, a global leader in providing trusted insights and analytics, is currently hiring for Associate Pharmacovigilance Specialist and Pharmacovigilance Specialist roles in Karnataka, India. These are hybrid positions offering a unique opportunity to work in a dynamic and supportive environment. If you have a background in life sciences, drug safety, or biomedical literature review, this could be your chance to join a world-class team. Read on to learn more about these exciting roles and how to apply.
Job Details
Position 1: Associate Pharmacovigilance Specialist
- Job ID: JREQ131104
- Location: Karnataka, India
- Job Type: Full-time, Permanent
- Work Mode: Hybrid
- Posted Date: March 3rd, 2025
- Working Hours: Monday to Friday, 11:00 AM – 8:00 PM IST
Position 2: Pharmacovigilance Specialist
- Job ID: JREQ131112
- Location: Karnataka, India
- Job Type: Full-time, Permanent
- Work Mode: Hybrid
- Posted Date: March 3rd, 2025
- Working Hours: Monday to Friday, 11:00 AM – 8:00 PM IST
About the Roles
As a Pharmacovigilance Specialist or Associate Pharmacovigilance Specialist at Clarivate, you will play a critical role in ensuring drug safety and compliance with pharmacovigilance regulations. Your primary responsibilities will include:
- Monitoring and reviewing biomedical literature for adverse event reporting.
- Identifying Individual Case Safety Reports (ICSRs) and other safety-relevant information.
- Writing accurate and concise summaries of biomedical case reports.
- Indexing and abstracting articles for inclusion in client-specific databases.
- Ensuring compliance with regulatory requirements and standard operating procedures.
- Maintaining awareness of new drugs, therapeutic categories, and biomedical terminology.
These roles require strong analytical skills, attention to detail, and the ability to work in a fast-paced environment.
Qualifications and Skills Required
For Associate Pharmacovigilance Specialist:
- Master’s degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, etc.).
- 1-2 years of experience in reviewing biomedical literature for adverse event reporting.
- Strong knowledge of biomedical terminology, drugs, and therapeutic areas.
- Excellent English language skills (comprehension, speaking, reading, and writing).
- Basic computer literacy.
For Pharmacovigilance Specialist:
- Master’s degree in Life Sciences, Health, or Biomedical Sciences.
- 4+ years of experience in biomedical literature review and adverse event reporting.
- Experience in indexing abstracts and providing feedback to primary screeners.
- Advanced knowledge of pharmacovigilance regulations and drug safety systems.
Additional Preferred Qualifications:
- Certification from a professional medical writer’s association.
- Experience with commercial and client-specific biomedical literature databases.
- Scientific or medical writing background.
Why Join Clarivate?
Clarivate is a global leader in providing trusted insights and analytics to accelerate the pace of innovation. By joining the PV Literature team, you will:
- Work in a supportive and collaborative environment.
- Receive personalized training and opportunities for professional growth.
- Engage in diverse aspects of pharmacovigilance and contribute to customer upgrade planning.
- Be part of a team that values innovation, diversity, and inclusion.
How to Apply
If you meet the qualifications and are excited about the opportunity to work with Clarivate, don’t wait! Apply now by visiting the official Clarivate careers page or clicking on the links below:
Apply for Associate Pharmacovigilance Specialist
Apply for Pharmacovigilance Specialist
