Pharmacovigilance Job at Clarivate
Looking for a pharmacovigilance career where you can work with biomedical literature and drug safety data? Clarivate is hiring an Associate Pharmacovigilance Specialist for a hybrid role in Karnataka, India. This Pharmacovigilance Job at Clarivate Careers is ideal for Life Sciences graduates and healthcare professionals interested in drug safety, adverse event reporting, and biomedical literature review. The role involves identifying Individual Case Safety Reports (ICSRs), writing scientific summaries, indexing biomedical data, and supporting global pharmacovigilance activities. Candidates with strong analytical skills and knowledge of medical terminology can build a rewarding career in patient safety and regulatory sciences. The position also offers exposure to global drug safety processes and scientific literature management.
About the Company:
Clarivate is a leading global company providing trusted insights, analytics, and workflow solutions across healthcare, life sciences, academia, and intellectual property sectors. The organization supports pharmaceutical and healthcare companies with biomedical research, drug safety, scientific information, and regulatory solutions. Clarivate is known for its innovation-driven environment, global operations, and strong focus on professional growth and knowledge services.
Job Details:
- Job Role: Associate Pharmacovigilance Specialist
- Location: Karnataka, India
- Work Mode: Hybrid
- Job ID: JREQ135672
- Industry: Pharmacovigilance / Life Sciences / Healthcare
- Posted Date: May 14, 2026
- Work Hours: Monday to Friday, 9 Hours
Key Responsibilities:
- Review biomedical literature for adverse event reporting
- Identify Individual Case Safety Reports (ICSRs)
- Analyze biomedical articles and drug safety alerts
- Write concise safety narratives and summaries
- Perform literature indexing and abstracting activities in this Pharmacovigilance Job
- Maintain accurate records in drug safety systems
- Assess safety-relevant information impacting drug risk-benefit profiles
- Select and summarize articles for literature databases
- Extract key scientific points from biomedical publications at Clarivate Careers
- Ensure timely completion of pharmacovigilance deliverables
- Maintain awareness of new drugs and therapeutic areas
- Support terminology maintenance and literature searches
Educational Requirements for this Job:
- Dentistry, Physiotherapy, or Nursing degrees with hospital exposure are advantageous
- 1–2 years of experience in biomedical literature review or pharmacovigilance preferred
- Equivalent experience in information science with drug safety knowledge may be considered
Skills Required:
- Strong understanding of pharmacovigilance and drug safety
- Knowledge of biomedical terminology and therapeutic areas
- Scientific and medical writing skills
- Ability to analyze and summarize biomedical case reports
- Attention to detail and accuracy in the literature review
- Good English communication and comprehension skills
- Knowledge of biomedical literature databases
- Analytical thinking and problem-solving abilities
- Time management and the ability to meet deadlines
- Flexibility to adapt to changing client requirements
- Familiarity with drug safety systems and regulatory processes
Benefits of the Pharmacovigilance Job:
- Hybrid work opportunity in Karnataka
- Exposure to global pharmacovigilance and biomedical literature processes
- Career growth in drug safety and regulatory sciences
- Opportunity to work with international healthcare and pharmaceutical clients
- Skill development in scientific writing and safety assessment
- Experience with biomedical databases and literature management
- Professional growth in the Life Sciences and Healthcare industry
- Collaborative and learning-focused work environment
- Opportunity to work on global patient safety initiatives
- Equal employment and career advancement opportunities.
