Amgen is seeking an experienced leader to head the global Study Evidence & Readiness function, shaping departmental strategy and overseeing TMF Operations and Inspection Readiness. You will ensure high-quality, compliant evidence across clinical studies and support regulatory readiness.
You will lead and develop global teams, manage budgets and resources, and drive continuous improvement of TMF processes. This role requires strong leadership, strategic thinking, and excellent stakeholder
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Director, TMF Operations & Inspection Readiness in Cambridge employer: Amgen
At Amgen, we pride ourselves on being a leading biotechnology company that prioritises the well-being and growth of our employees. As an EU Regulatory Affairs Manager, you will be part of a diverse and inclusive team dedicated to serving patients, with ample opportunities for professional development and a generous Total Rewards Plan. With flexible working arrangements from our offices in Cambridge, Uxbridge, or Lisbon, you can enjoy a fulfilling career while maintaining a healthy work-life balance.
