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You would 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
Act as a scientific and clinical expert in diabetes and CGM, ensuring the organisation remains at the forefront of emerging evidence and practice. Provide authoritative, evidence-based guidance on clinical data, device utilisation, and patient management
Primary responsibilities include medical and safety oversight of clinical trials as well as corporate support for business opportunities. The Medical Director provides Medical Monitoring services to clinical trials with the aim to monitor the safety and
Provide field-based medical support to Sobi’s clinical research programs, registries, and facilitation of the investigator-initiated research process. Communicate key medical insights from KOLs/HCPs to inform refinement of medical strategies or tactics;