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Amgen Clinical Research Pharmacy Services Manager in London, United Kingdom


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.



What you will do

In this vital role you will support Global Development Operations (GDO) to ensure Investigational Product (IP) Management processes and the clinical site perspectives are understood and integrated into Amgen Clinical Trial design and execution.

Key responsibilities:

  • Support the execution of the strategic direction of Clinical Research Pharmacy Services (CRPS) to ensure safe, high quality and compliant Clinical Trial execution

  • Ensure quality, identify and mitigate risks within studies for IP management processes, documentation and training

  • Advise and support key stakeholders to ensure IP Management practices are followed at global sites in line with Good Clinical Practices (GCP), ensuring patient safety, data integrity and to safely incorporate these practices into clinical trial design

  • Author IP related documentation (e.g. Investigational Product Preparation and Administration (IPPA), Dose Preparation Worksheets and Training Materials) as required for study support and delivery

  • Assist in developing training tools for clinical sites for studies with complex dosing regimens and support delivery of site training where required

  • Act as the primary point of contact on behalf of Amgen for study related IP Management questions and support site challenges seen with IP administration, formulation preparation, labelling and/or packaging

  • Provide input and support into the design of IP sections of study protocols

Be part of our team

You would be joining a continuously growing team within R&D, working in a global and cross functional manner. You will assist Clinical Program Operations (CPO), Global Study Operations - Site Management (GSO-SM) and GDO.


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 expert professional, are these qualifications and skills:

  • Degree educated in Pharmacy, Nursing or equivalent

  • Broad work experience in life sciences or medically related field, including biopharmaceutical clinical research experience acquired by working on clinical trials

  • Practical experience in a clinical research setting working on sophisticated clinical programs in a pharmacy at an investigational site

  • Knowledge of ICH/GCP regulations and guidelines

  • Experience with drug formulations, sterile product compounding and administration practices

  • Proven ability to anticipate and resolve problems as well as experience introducing new processes or services

  • Ability to write, communicate and present clearly using scientific and clinical issues terminology

  • Computer and system operation skills


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 fully remote, or, if situated near an office, the option to work flexibly from home with occasional office presence at our Cambridge or Uxbridge next-generation workspace.


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.

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.​