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Director, Vaccines Medical Program Management About the role Provide strategic program leadership for the most critical and complex Medical priorities, ensuring that enterprise Medical strategies are translated into executable portfolio plans, governed effectively, and delivered with visibility, accountability,
CSL’s R&D organization is accelerating innovation to deliver greater impact for patients. The Associate Director, Regulatory Project Manager role is based in our Glattbrugg, Switzerland office, with hybrid onsite three days a week, and coordinated with
Takeda Pharmaceuticals International AG in Switzerland seeks a Director, Vaccines Medical Program Management to lead end‑to‑end execution of the most strategic medical portfolios, establishing integrated roadmaps, governance, and escalation pathways.You will partner with senior medical leaders to shape
Position Summary The Senior Director, Head of Medical Evidence reports into the Vice President, Head of Disease Areas and coordinates with Medical Affairs and cross-functional stakeholders to lead the Integrated Evidence Generation Plans (IEGP) for all
The Director Non-Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations. The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology, PK/QSP, and toxicology
Job Description Location: While a primarylocation is identified for this role, qualified internal candidates located in Cambridge, MA, USA may also be considered, subject to business needs, role requirements, talent availability, and local legal requirements. Compensation:
Takeda in Switzerland is seeking a senior leader to drive Global Patient Access (GPA) strategy and operations. You will influence cross-functional stakeholders to deliver integrated patient-centric strategies aligned with regulatory and product lifecycle needs.You will leverage