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Clarivate Hiring Freshers for Pharmacovigilance Role
Clarivate
Noida (Hybrid)
Freshers Eligible
Drug Safety
ICSR & Literature Review
Full-Time
📌 Job Overview
Position: Associate Pharmacovigilance Specialist
Location: Noida, India (Hybrid)
Experience: Fresher / 0–2 Years
Industry: Pharmacovigilance & Drug Safety
Work Hours: 9 AM – 6 PM / 11 AM – 8 PM
🔬 Key Responsibilities
- Review biomedical literature for Individual Case Safety Reports (ICSRs)
- Identify adverse events and safety signals
- Write concise safety narratives
- Perform literature monitoring as per regulatory requirements
- Evaluate drug labels & therapeutic safety information
- Maintain audit-ready safety documentation
- Ensure compliance with global pharmacovigilance standards
🎓 Eligibility & Skills
- Master’s degree in Pharmacy, Biotechnology, Microbiology, Biochemistry, Biomedical Sciences or Pharm.D
- Fresher OR up to 2 years experience in literature review / PV
- Strong biomedical terminology knowledge
- Understanding of pharmacovigilance regulations
- Familiarity with PubMed / Embase databases
- Strong analytical & writing skills
💰 Salary (Estimated)
₹3.5 LPA – ₹5.5 LPA
🌍 Why Join Clarivate?
- Structured pharmacovigilance training
- Exposure to global drug safety standards
- Hybrid work flexibility
- Career growth in PV & biomedical review
- Work with global pharmaceutical clients
Before applying, you can improve your understanding of pharmacovigilance concepts and drug safety reporting by attempting this quick quiz.
📌 Note Before You Apply:
Read the job description carefully and ensure your qualifications align with pharmacovigilance literature review and drug safety requirements.
Read the job description carefully and ensure your qualifications align with pharmacovigilance literature review and drug safety requirements.
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