Clarivate Hiring Associate Pharmacovigilance Specialist | Pharma Graduates Apply
Looking for a Pharmacovigilance Job with a global healthcare intelligence company? Clarivate Careers has announced an excellent opportunity for an Associate Pharmacovigilance Specialist in Karnataka, India. If you have experience in drug safety, biomedical literature review, medical writing, or pharmacovigilance, this hybrid role offers an outstanding opportunity to grow your career with one of the world’s leading life sciences organisations.
- Job Title: Associate Pharmacovigilance Specialist
- Location: Karnātaka, India
- Remote: Hybrid
- Job ID: JREQ135671
About the Company
Clarivate is a global leader in providing trusted intelligence and innovative solutions across life sciences, healthcare, academia, and intellectual property. Through Clarivate Careers, professionals gain opportunities to work on cutting-edge healthcare and pharmacovigilance projects while contributing to patient safety worldwide.
Job Description
The Associate Pharmacovigilance Specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.
Key Responsibilities
- Review biomedical literature and identify Individual Case Safety Reports (ICSRs) and other drug safety information.
- Summarize safety findings and prepare concise case narratives.
- Evaluate drug safety using product labels and regulatory guidelines.
- Perform accurate and timely literature safety reviews.
- Record all safety assessments in the drug safety system for audit purposes.
- Select relevant scientific articles for the client’s literature database.
- Prepare clear and detailed abstracts of selected articles.
- Index and organize article information for easy retrieval.
- Complete indexing and abstracting within regulatory timelines.
- Stay updated on new drugs, therapeutic areas, diseases, and medical terminology.
- Support literature searches and terminology maintenance as required.
Qualification
- Master’s Degree in Pharmacy
- At least 1-2 years of experience reviewing biomedical literature for adverse event reporting.
- Related experience in drug safety/ pharmacovigilance is desirable.
- Strong analytic ability to analyse and summarize the main points of biomedical case reports, studies, or specific topics.
- At least 1 year of experience using writing skills to support the creation of succinct, accurate, and precise summaries.
- At least 1 year of working knowledge of biomedical terminology, drugs, and therapeutic areas.
Skills Preferred
- Certification from a professional medical writer’s association.
- Experience with commercial and client-specific biomedical literature databases.
- Scientific/medical writing background.
- Excellent English language skills (comprehension, speaking, reading, and writing).
- Flexibility and adaptability to changing client needs.
