Amgen is seeking a Director of Study Evidence and Readiness to define strategy for TMF operations, drive inspection readiness, and partner with global teams to ensure regulatory compliance across the clinical portfolio.
You will lead and develop cross-functional teams, oversee audits, manage budgets and resources, push continuous improvement in TMF processes, and deliver strategic insights to senior leadership on evidence quality, risks, and study trends.
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Director, TMF Strategy & Inspection Readiness 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.
