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
📌 Drug Safety Associate (Gujarat)
🏢 Refined Reports Data
📍 Gujarat
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