Offer summary

Qualifications:

6+ years of relevant clinical research experience in a pharmaceutical company or CRO, ideally in Biometrics, Data Management, or Statistical Programming., Strong understanding of the clinical research process and data generation, analysis, and reporting., Excellent computer skills, particularly in Microsoft Excel, including functions and formulas., University/college degree in a life science preferred. .

Key responsibilities:

Develop accurate initial budget assumptions based on RFPs and available protocols.

Build and maintain a dynamic pricing tool to support project deliverables and client expectations.

Lead cross-functional budget reviews and ensure strategic alignment.

Independently write and deliver high-quality budgets, ballparks, and change orders.

Job description

FORTREA: WHERE MEDICAL BREAKTHROUGHS BEGIN

Imagine the impact. Every team at Fortrea’s Clinical Pharmacology is driven by one question: Will this new medicine be safe? The data we generate in phase I clinical research ends up on a drug’s label —your expertise will help turn ideas into real treatments for patients in need.

As part of our ongoing evolution, we're introducing a new team structure and opening our first UK-based Pricing Manager role. You'll shape pricing strategies for the Biometrics function in early-phase clinical trials, ensuring budgets align with the project delivery strategy.

Permanent, full-time, home-based job anywhere in the UK

WHAT YOU´LL DO

On a typical day you may expect:

Develop accurate initial budget assumptions for deliverables based on Request for proposals (RFP) and/or available protocols, synopsis or client input.
Build and maintain a dynamic pricing tool that supports Fortrea´s understanding of the project deliverables and client’s expectations and reflects evolving project needs and changes.
Lead cross-functional budget reviews, coordinating input from functional leads and SMES and ensuring consistency and strategic alignment.
Independently lead writing and delivery of high-quality full budgets, ballparks, change orders and re-costs estimates.
Provide expert insight for Biometrics expectations and deliverables during RFP process (e.g., assumption development, team discussions, and bid defense preparation)

WHO YOU´LL WORK WITH

You’ll collaborate closely with colleagues across Sales, Data Management, Statistical Programming, Biostatistics, Medical Writing, Pharmacokinetics, and more. Expect variety, visibility, and the chance to influence early-stage trial design.

WHAT YOU´LL BRING

To succeed in this job, you must bring a strong understanding of the clinical research process and how clinical data is generated, analyzed and reported. We need you to bring:

6+ years of relevant clinical research experience in a pharmaceutical company or CRO, ideally in Biometrics, Data Management or Statistical Programming.

Backgrounds in such roles as Medical Writing, Clinical Research Nursing, or Clinical Operations (e.g. SCRA, Clinical Team Leads, Project Managers…) are also welcome.

Excellent computer skills, especially Microsoft Excel (particularly functions and formulas)

University/college degree (life science preferred)

Confidence working independently and collaboratively across teams

UK residency and right to work — we’re unable to sponsor this role

WHY JOIN FORTREA

At Fortrea, you won’t just be part of a project — you’ll be part of a purpose. You’ll see the results of your work in real time, and when a drug you’ve helped price and plan gets approved, you’ll know you made a difference.

Join us on our mission to bring life-changing healthcare solutions to patients around the world.

#LI-CV1 #LI-Remote

Learn more about our EEO & Accommodations request here.

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