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Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity; Work cross functionally to ensure clinical strategy is translated into the
You will be a contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE
Understands and keeps updated with the pre-clinical, clinical pharmacology and data relevant to the molecule of interest. Knowledge on antibody is a plus; Critically reads and evaluates relevant medical literature with deep understanding of the data and