Perform case processing of Adverse Event (AE) reports from various sources (spontaneous, literature, clinical trials).
Enter and update safety data into safety databases with accuracy and timeliness.
Assist in narrative writing and medical coding of adverse events using MedDRA.
Conduct literature screening for safety information as per regulatory requirements.
Ensure compliance with global regulatory requirements and internal standard operating procedures (SOPs).
Support in preparing periodic safety update reports (PSURs) and risk management documents.
Collaborate with cross-functional teams such as medical writing, regulatory affairs, and clinical research.
Bachelor's or Master's degree in Pharmacy, Life Sciences, Medicine, Nursing, Biotechnology, or related discipline.
Job Types: Full-time, Permanent, Fresher
Pay: ₹360,344.96 - ₹578,383.71 per year
Benefits:
Health insurance
Paid sick time
Work Location: In person
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