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Pharmacovigilance careers continue to grow rapidly in India, especially for professionals skilled in drug safety, literature screening, and case processing. Clarivate has opened applications for an Associate Pharmacovigilance Specialist in Noida, offering a hybrid work model and an excellent opportunity to build a strong career in PV operations.
If you have 1 year of pharmacovigilance experience, especially in literature surveillance, this role is a perfect fit.
⭐ Key Responsibilities
As an Associate Pharmacovigilance Specialist, you will:
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- Evaluate global medical and scientific literature for potential adverse events, safety concerns, and case reports requiring follow-up.
- Identify and extract relevant safety data, including ADRs, safety signals, and clinical findings.
- Enter extracted data into pharmacovigilance databases with accuracy and compliance.
- Maintain clear and organized documentation for PV literature screening activities.
- Stay updated with global pharmacovigilance regulations, guidelines, and best practices in signal detection and drug safety.
🎓 Minimum Qualifications
- Bachelor’s degree in Pharmacy, Life Sciences, Nursing, or a related field
- Minimum 1 year experience in pharmacovigilance literature screening or PV case processing
- Good understanding of medical terminologies and scientific literature
- Strong attention to detail and documentation skills
💼 Why Join Clarivate?
- Work with a global leader in life sciences analytics
- Hybrid working environment (Noida)
- Opportunity to grow in drug safety, signal detection, and pharmacovigilance operations
- Exposure to global safety standards and regulatory guidelines
📌 How to Apply
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