Clarivate is hiring an Associate Pharmacovigilance Specialist in Noida, Uttar Pradesh (Hybrid mode) for candidates with a Master’s degree in Life Sciences and up to 2 years of experience in pharmacovigilance or biomedical literature review.
This opportunity is ideal for freshers and early-career professionals seeking to build a career in pharmacovigilance jobs in India, particularly in ICSR processing, biomedical literature monitoring, and drug safety review.
📌 Job Overview
- Position: Associate Pharmacovigilance Specialist
- Location: Noida, Uttar Pradesh, India
- Work Mode: Hybrid
- Experience: Fresher / 0–2 years
- Industry: Pharmacovigilance / Drug Safety / Life Sciences
- Posted On: 16 February 2026
This Associate Pharmacovigilance Specialist job in Noida focuses on biomedical literature monitoring, adverse event identification, and safety narrative writing in compliance with global pharmacovigilance regulations.
🔬 Key Responsibilities – Pharmacovigilance Role
The Associate Pharmacovigilance Specialist will:
- Critically analyze biomedical literature for Individual Case Safety Reports (ICSRs)
- Identify adverse events and other safety-relevant information
- Perform biomedical literature monitoring as per regulatory requirements
- Write concise safety narratives summarizing ICSR criteria
- Assess drug labels and therapeutic area information for safety evaluation
- Ensure timely and accurate drug safety review
- Maintain audit-ready documentation in drug safety databases
- Adhere strictly to SOPs and pharmacovigilance compliance standards
This pharmacovigilance job requires strong analytical ability and familiarity with medical terminology and therapeutic areas.
🎓 Eligibility & Qualifications
To apply for this Clarivate Pharmacovigilance Specialist job, candidates must have:
- Master’s Degree in:
- Pharmacy
- Microbiology
- Biotechnology
- Biochemistry
- Biophysics
- Life Sciences or Biomedical Sciences
- Experience:
- Fresher OR up to 2 years in biomedical literature review for adverse event reporting
- Experience in pharmacovigilance literature screening preferred
- Skills Required:
- Strong understanding of biomedical terminology
- Knowledge of pharmacovigilance regulations
- Analytical and summarization skills
- Familiarity with literature databases (PubMed, Embase, etc.)
- Excellent written and verbal English communication
- Effective time management and adherence to SOPs
🏢 About the Pharmacovigilance Team
The Pharmacovigilance team at Clarivate supports multiple global clients across therapeutic areas. Employees receive:
- Structured pharmacovigilance training
- Exposure to global drug safety standards
- Opportunities in biomedical literature monitoring
- Client engagement and safety compliance projects
- Supportive and growth-oriented work environment
⏰ Working Hours
- 9:00 AM – 6:00 PM IST
OR - 11:00 AM – 8:00 PM IST
- Monday to Friday
- Hybrid work mode (Noida / Bangalore base)
💰 Salary & Benefits (Estimated)
For Associate Pharmacovigilance Specialist roles in Noida, the expected salary range is:
- ₹3.5 LPA – ₹5.5 LPA (CTC) depending on experience and skill set
Additional benefits may include:
- Hybrid flexibility
- Professional training programs
- Career progression in drug safety
- Exposure to global regulatory frameworks
🚀 Why This Job is Important for PV Career Aspirants
This pharmacovigilance job for freshers in Noida is highly suitable for candidates targeting:
- ICSR processing roles
- Biomedical literature review jobs
- Drug safety associate positions
- Entry-level pharmacovigilance careers in India
Working with Clarivate provides exposure to global safety databases and regulatory-compliant literature monitoring processes, which are critical competencies in the pharmacovigilance industry.
📩 How to Apply
