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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
Define medical strategy in line with company ambition and cluster scorecard/priorities. Assess, design, and lead all medical activities including research programs, clinical trials, RWE programs, data mining projects, and all data generation activities.
You will provide communication expertise and lead a strategy-driven approach to authoring of key clinical and regulatory documents and regulatory submissions, to ensure clarity, credibility and consistency of clinical information throughout submission