Roles & Responsibilities of Pharmacovigilance

A Drug Safety Associate is a professional who works in the field of pharmacovigilance within a pharmaceutical, biotechnology, medical company or life sciences consulting firm. The main role of a Drug Safety Associate is to monitor the safety of drugs and medical devices once they are on the market and ensure that they are being used safely.

- Reviewing and evaluating adverse event reports (AERs) to determine if they meet regulatory reporting requirements.
- Entering and maintaining adverse event information in safety databases
- Narrative writing
- Communicating with healthcare professionals and other stakeholders to gather additional information about adverse events
- Assisting in the preparation of safety reports to be submitted to regulatory agencies
- Monitoring safety literature to stay current on the latest safety information related to the company's products




- Collaborating with other departments such as clinical research, regulatory affairs, and pharmacovigilance to ensure compliance with safety regulations and guidelines
- Participating in the development and implementation of safety policies and procedures
- Reviewing and assessing the safety profile of new and existing products
- Participating in the development and execution of risk management plans
- Communicating with regulatory authorities, healthcare professionals, and other stakeholders on safety-related issues.

Job Types: Full-time, Permanent, Fresher

Pay: ₹25,064.34 - ₹35,471.11 per month

Advantages:

- Health insurance
- Paid sick time
- Provident Fund

Work Location: In person

📌 Pharmacovigilance (Nagpur)
🏢 Refined Reports Data
📍 Nagpur