Job Information
Amgen Clinical Pricing Manager in Cambridge, 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 read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
CLINICAL PRICING MANAGER
LIVE
What you will do
Let’s do this. Let’s change the world. In this vital role you will provide Clinical Trial Budget design, strategy and payment oversight to Clinical Study Teams at a study, product and therapeutic area level for the purpose of operationalizing a clinical study or program.
You will be responsible for:
Providing oversight at a Product or Therapeutic Area of pricing proposal creation for Clinical studies
Providing oversight of development and periodic monitoring of study level budget estimates
Budget strategy and design including fair market value negotiation guidelines
Providing oversight of payment system configuration including Electronic Data Capture (EDC) to payment schedule mapping
Ensure site budgets for studies within assigned TA / Product are tracked in Pricing & Payments database
Participating in team and department special projects as required
Maintain knowledge and oversight for issues involving all therapeutic areas assigned
Key activities:
- Department processes and procedures
Provide Oversight and Coordination of all Pricing & Payment Activities for assigned therapeutic area including:
Pricing requests from Study Clients for original and/or amended protocols
Budget worksheet creation and corresponding documentation
Determining EDC payment triggers and build EDC budget mapping
Pricing and negotiation strategy
Budget Strategy and Kick-Off meetings with GSM and GSO
Maintain database of pricing and related data for use in cycle time, site selection and negotiation analysis and reporting
Site budget escalations providing guidance to budget negotiators and Clinical Study Teams as needed
Clinical Trial Payment System configuration including rules for EDC payment triggers and approval rules for manual payments
Site configuration package creation for Clinical Trial Payment System (CTPS)
Approval of manual payment requests for sites using the CTPS
Approval site invoices for sites using the Site Invoice Upload model within CTPS
Creation of Payment Information Guide for each study and provide support for LOC where Payment Log Optimization Tool is used
Close out activities for sites paid via the CTPS
Maintenance of study specific status trackers for assigned studies
Issue resolutionwith CTPS vendor for any escalated site issues
- Department metrics and related data
Primary point of contact and responsible for budget oversight and true up of patient cost budgets at the study and therapeutic area level
Preparation of ad hoc reports relating to dept metrics, performance, or other data for management, as needed
- Systems and vendor support
Provide oversight and assistance as needed with technical requirements and vendor relationship management for systems used, including management of vendor agreements and upgrades
Be part of our team
The Clinical Pricing & Payments team is a diverse international team within R&D Global Development Operations that is responsible for Investigator Grant budgets and payments process. We are also responsible for Fair Market Value (FMV) assessment of Investigator Sponsored Studies. The team works in a dynamically changing environment implementing innovative system and process solutions.
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:
Bachelors degree or equivalent
Broad work experience in financial support or contract or budget administration role, preferably in within the clinical field
Experience working in a global, matrix organization
Proficiency in anticipating and resolving problems
Knowledge and experience with principles of fair market value and payments to investigators
Prioritisation/organisation skills
Working under multiple and competing deadlines
Excellent written and verbal communication skills
Data analysis skills
Very proficient with basic computer programs, such as Microsoft Excel
Experience with databases
Ability to work as part of cross-functional team as part of a short-term project or goal
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.
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
Apply now
Objects in your future are closer than they appear. 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.