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Lead the analytical and medical evaluation of emerging aggregate safety data from pre‑clinical and clinical studies to establish the product’s early safety profile
Solve unique and complex safety challenges that impacts patient surveillance and business decisions
Collaborate closely with the non‑clinical project manager, medical specialist, and clinical pharmacologist to develop scientifically strong study designs with ambitious timelines
Chair a cross‑functional drug safety committee and ensure high‑quality safety input across development activities
Prepare benefit–risk communication, contribute to clinical study designs and protocols, and represent Safety Surveillance in cross functional teams
Identify and drive initiatives that strengthen scientific and strategic excellence in safety surveillance while working independently and with skilled colleagues across Non‑clinical and Clinical Development
Safety Surveillance Principal Specialist
Søborg, Capital RegionDKK847K - DKK1,245K / yearPosted 1 weeks ago
Full-timeprincipal