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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
Ensuring the highest quality standards from subcontractors in line with current regulations and good practices (GxP), and delivery of reliable clinical data within agreed timelines. Oversight of early‑phase clinical trials (Phase I–II) in
You will be responsible for providing medical safety expertise for the benefit/risk assessment of products in clinical development, with a specific focus on our key biologic (Nemolizumab). This involves signal detection, risk management, risk
Provide strategic medical leadership across CEE in alignment with global and regional priorities; Lead and inspire regional medical team; Drive CEE regional medical strategy and execution in alignment with Sobi’s global and brand priorities
Build and manage long term relationships with key physicians, sites and partners while also leading medical strategy and tactics across our diverse geographic locations. This individual will be a strategic partner to indirect affiliates as well as