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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
Collaborating with Medical Experts and Key Opinion Leaders to solve scientific and clinical challenges, including providing up‑to‑date medical support on Alcon products; Leading scientific exchange through presentations, congress participation, and
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
Create expert medical and scientific inputs for biosimilar products and programs; Maintain general scientific expertise, including up-to-date knowledge of international guidelines and requirements for biosimilars; Prepare and deliver high-quality internal
Play a key role in the design, execution, and evaluation of Phase 1, 2, and 3 clinical trials, providing subject‑matter expertise in pediatric viral infectious diseases. This role will support the development and registration of novel therapies for