Remote Associate Director, Global Clinical Programs

Amgen SA

Uxbridge

Hybrid

GBP 120,000 - 155,000

Full time

5 days ago
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Benefits offered by this job

Hybrid work option

Job summary

Amgen in the United Kingdom seeks an Associate Director of Global Clinical Program Management to lead the operational delivery of complex clinical studies across multiple geographies, ensuring timelines, budget, quality and strategy are met.

You will line-manage Study Delivery Leads, manage program-level budgets and vendors, partner with CROs and local execution teams, and provide strategic input on study design, enrolment, diversity and patient-centric approaches.

Qualifications

  • Degree educated.
  • Experience managing people or teams.
  • Life sciences or biopharma clinical research experience.
  • Experience across multiple geographies.
  • Experience with CROs and outside vendors.

Responsibilities

  • Lead the operational planning and delivery of multiple clinical studies or programs across geographies, ensuring timelines, budget, quality and strategy are met.
  • Proactively identify delivery risks and guide course-correction to keep studies on track.
  • Drive consistent, high-quality operational practices across all assigned studies and programs.
  • Line-manage and develop Study Delivery Leads, setting clear objectives and fostering high performance.
  • Oversee program-level issues, risks, and escalation, ensuring timely and effective resolution.
  • Partner cross-functionally and with local execution teams to align priorities, resources, and delivery plans.

Skills

Leadership
Team management
Program management
Clinical research
Vendor management

Education

Degree educated

Job description

Amgen in the United Kingdom seeks an Associate Director of Global Clinical Program Management to lead the operational delivery of complex clinical studies across multiple geographies, ensuring timelines, budget, quality and strategy are met.

You will line-manage Study Delivery Leads, manage program-level budgets and vendors, partner with CROs and local execution teams, and provide strategic input on study design, enrolment, diversity and patient-centric approaches.

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