Global Clinical Program Resource Management (PRM), Manager
AmgenUnited kingdom - aberdeenUpdate time: March 11,2022
Job Description

Career Category

Clinical

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

Global Clinical Program Resource Management (PRM), Manager

LIVE

What you will do

In this vital role you will contribute to oversight of Global Clinical Program Management (GCPM) resourcing and also GCPM’s Functional Service Providers (FSPs). In addition, you will support the Program Resource Management (PRM) Senior Managers in training, standardization activities and development of operational efficiencies and continuous improvement initiatives within GCPM which also impact the wider Global Development Operations (GDO) function.  

  • Contribute to and support resource management related activities for Global Clinical Trial Managers (GCTMs), Regional Clinical Trial Managers (RCTMs), Clinical Trial Specialists (CTS’) and Study Management Associates (SMAs), both FTE and FSP staff
  • Support the resource allocation and program assignments of GCTM staff
  • Contribute to the development of GCPM operational efficiency and training
  • Ensure GCPM staff adherence to operating standards and promote standardization and best practice sharing to ensure operational compliance
  • Provide input into GCPM training and develop standards authorship and/or review
  • Lead staff-focused process improvement initiatives

Be part of our team

You would be joining the Global Clinical Program Management team which is part of the Global Development Operations function at Amgen.

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:

  • BS/BA/BSc in the sciences or RN
  • Extensive work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company
  • Previous management experience of direct reports
  • Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)

Knowledge:

  • Advanced knowledge of global clinical trial management
  • Clinical trial processes and operations
  • Extensive knowledge of ICH/GCP regulations and guidelines
  • Project and Program management including oversight of study deliverables
  • Time, cost and quality metrics
  • Understanding of resource management and organizational capacity
  • Experience in line and people management
  • Experience in developing goals and training plans to maximize talent and career development of staff

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
  • Flexible working from home policy.

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, colour, 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.

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