The responsibilities for this role include collecting and analyzing data on adverse drug reactions (ADRs) from clinical trials and post-market surveillance, preparing and submitting safety reports to regulatory authorities, ensuring compliance with pharmacovigilance regulations and guidelines, collaborating with healthcare professionals to assess and manage drug-related risks, and maintaining and updating safety databases with accurate information. Key skills required for this position are attention to detail for precision in analyzing and documenting safety data, regulatory knowledge including familiarity with FDA, EMA, and ICH-GCP guidelines, communication skills to effectively convey safety findings, analytical thinking for assessing risks and identifying safety signals, and team collaboration for working with cross-functional teams in pharmacovigilance. This is a full-time job opportunity with benefits including health insurance and provident fund. The work location for this position is in person.,

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Pharmacovigilance Associate