Pharmacovigilance Associate

0 years

3 - 0 Lacs

Posted:5 days ago| Platform: SimplyHired logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • 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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