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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
You will play a key part in driving operational excellence, ensuring compliance, and enabling seamless execution of strategic initiatives - from managing external events and vendor relationships to supporting budgeting processes and global collaboration.
They will lead and develop the hematology medical team, setting direction and fostering a culture of medical excellence, defining and implementing medical affairs therapeutic area (TA) strategy for hematology, aligned with affiliate and global priorities.