Pharmacovigilance Job Opportunity at Clarivate | High-Growth Pharma Job Role | Apply Now
Explore a high-growth Pharmacovigilance Job opportunity in the life sciences sector, ideal for candidates seeking a strong foundation in drug safety and biomedical literature review. This Pharma Job role as an Associate Pharmacovigilance Specialist offers hands-on experience in pharmacovigilance services, adverse event reporting, and scientific literature analysis, making it a great step toward a rewarding career in healthcare and research domains.
- Job Title: Associate Pharmacovigilance Specialist
- Location: Karnātaka, India
- Remote: Hybrid
- Job ID: JREQ135672
About the Company
Clarivate is a global leader in life sciences, healthcare, and research solutions, supporting organizations with innovative insights and scientific expertise. The company provides opportunities for professionals in pharmacovigilance, drug safety, and biomedical research while fostering an inclusive and growth-oriented work environment.
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, medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.
Key Responsibilities
- Analyze biomedical literature and drug safety alerts for ICSRs and safety-related information.
- Write summaries and narratives for identified safety cases.
- Perform safety assessments using knowledge of client drug labels.
- Complete drug safety reviews within quality and timeline standards.
- Maintain audit-ready records using drug safety systems.
- Select relevant articles for client literature databases.
- Prepare accurate abstracts and article summaries.
- Extract and index key literature points for easy retrieval.
- Ensure timely indexing and abstracting as per regulatory deadlines.
- Stay updated on new drugs, therapeutic areas, and biomedical terminology.
- Support additional literature searches and terminology maintenance activities.
Qualification
- Master’s Degree in Pharmacy
- At least 1-2 years of experience reviewing biomedical literature for adverse event reporting.
- OR equivalent combination of education and experience (e.g., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety).
- Related experience in drug safety/pharmacovigilance is desirable.
- Strong analytic ability to analyze and summarize the main points of biomedical case reports, studies, or specific topics.
- At least 1 year of experience using writing skills to create succinct, accurate, and precise summaries.
- At least 1 year of working knowledge of biomedical terminology, drugs, and therapeutic areas.
Preferred Qualification
- 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.
