Director Clinical Program Resource Management
Director Clinical Program Resource Management
United Kingdom - London Apply NowLOCATIONS: United Kingdom - Cambridge WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Feb. 25, 2025 CATEGORY: Clinical
HOW MIGHT YOU DEFY IMAGINATION?
At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission—to serve patients—has driven our status as one of the world’s preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge partnerships that advance the biotechnical and biopharmaceutical science that can turn the tide of serious, life-interrupting illnesses.
DIRECTOR CLINICAL PROGRAM RESOURCE MANAGEMENT
LIVE
What you will do
In this vital role you will oversee and manage global Clinical Program Operations (CPO) resources and Functional Service Provider (FSP) performance. The role includes translating business strategy into effective resource planning, supporting standardization and efficiency, driving continuous improvement initiatives within the CPO function and its interactions with Global Development Operations (GDO) function.
- Recruitment, line management, performance management and mentoring of Program Research Management (PRM) staff
- Global-level functional oversight of the CPO roles (e.g. Global Trial Manager, Local Trial Manager)
- Coordinate FSP performance and resource allocation
- Lead strategic staff-focused process improvement and training initiatives
- Contribute to risk assessment and mitigation
- Partner with stakeholders and external suppliers
- Support CPO goal setting, drive operational efficiency and onboarding
WIN
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:
- Degree educated
- Experience in life sciences or medical field, including biopharmaceutical clinical research with a sophisticated knowledge of global clinical trial management and ICH/GCP regulations
- Previous managerial/leadership experience and oversight of clinical research vendors
- Project, program and resource management skills as well as organizational capacity
- Time, cost and quality metrics
- Experience in developing goals and training plans for staff development
THRIVE
What you can expect of us
As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.
- Vast opportunities to learn and move up and across our global organization
- Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
- Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
LOCATION: Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.
Application close date 11th March 2025
APPLY NOW
for a career that defies imagination
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
careers.amgen.com
Equal Opportunity Statement
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
