Description
SUMMARY: * Proficient in ARGUS Data Safety submission and Narrative Writing * Thorough understanding and knowledge of MedDRA coding, pharmacovigilance practices for both Clinical Trial and Post marketing AE reporting * Well versed with GVP-ICH guidelines * ECFMG certified medical graduate with strong clinical knowledge * Self-driven, highly motivated medical professional with excellent leadership and organizational skills * Works well in stressful environment to meet deadlines by leading teams in an independent, self-directed manner
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