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
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