- Process and evaluate Individual Case Safety Reports (ICSRs) received from various sources.

- Perform data entry, case triage, case processing, and follow-up of adverse event reports.

- Review medical literature for potential adverse drug reactions.

- Identify and document Adverse Events (AEs), Serious Adverse Events (SAEs), and Adverse Drug Reactions (ADRs).

- Perform medical coding using tools such as MedDRA and WHO Drug, as applicable.

- Assess cases for seriousness, expectedness, and causality according to company procedures.

- Prepare and maintain accurate pharmacovigilance documentation.

- Follow company SOPs, GVP guidelines, and regulatory requirements.

- Support quality review and reconciliation activities.

- Maintain confidentiality and ensure data accuracy within safety databases.

- Communicate with internal teams and, when required, follow up for missing case information.

Pay: ₹300,000.41 - ₹450,000.17 per year

Benefits

- Cell phone reimbursement

- Versatile schedule

- Food provided

- Paid sick time

- Provident Fund

Work Location: In person

📌 Pharmacovigilance Associate (Pune)
🏢 Klinscience Healthcare
📍 Pune