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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 play a key role in shaping impactful medical affairs activities. Working at the forefront of CGM innovation, you will collaborate closely with healthcare professionals and distributors to translate strong clinical evidence into meaningful
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