Responsibilities:
- Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post-marketing surveillance.
- Ensure compliance with regulatory guidelines for drug safety reporting.
- Prepare and submit safety reports to regulatory authorities.
- Collaborate with healthcare professionals to assess and manage drug-related risks.
- Maintain and update safety databases with accurate information.
Key Skills:
- Attention to Detail: Precision in analyzing and documenting safety data.
- Regulatory Knowledge: Familiarity with FDA, EMA, and ICH-GCP guidelines.
- Communication Skills: Ability to convey safety findings effectively.
- Analytical Thinking: Assessing risks and identifying safety signals.
- Team Collaboration: Working with cross-functional teams in pharmacovigilance.
Job Type: Full-time
Pay: ₹350,000.00 - ₹975,000.00 per year
Benefits:
- Health insurance
- Provident Fund
Work Location: In person
