Clinical Pricing Manager

Career CategoryClinical Development

Job Description

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:

1. 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 resolution with CTPS vendor for any escalated site issues

2. 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

3. 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.

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