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Develop and implement the Global Medical Affairs plan for PsO aligned with biologics portfolio strategy, with emphasis on post-launch lifecycle optimization; Ensure tactical execution of medical plans within agreed global priorities and governance
Use innovative regulatory approaches and provide strategic regulatory guidance for assigned projects/products. Develop and implement regulatory strategies, integrating inputs from regulatory team and cross functional partners to build globally aligned
Develop and drive the nonclinical PKPD strategy for projects. Ensure translation from in vitro data and in vivo nonclinical studies to prediction of efficacy and safety in patients. Build PKPD models of sufficient complexity to allow hypothesis testing
Build and coordinate early-stage small-molecule discovery project teams, owning strategy, prioritization, and key go/no-go decisions - from hit finding to early lead optimization, towards valorization; Drive the integration of computational methods into
The successful candidate will bring a strong track record in global medical affairs, experience supporting product launches, exceptional scientific acumen, and the ability to influence stakeholders across diverse functions and geographies. This role