Job Information
Amgen Clinical Research Pharmacy Services Manager in London, United Kingdom
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.
CLINICAL RESEARCH PHARMACY SERVICES MANAGER
LIVE
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.
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 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
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 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.
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.