Senior Director, IT Products, Clinical Pharmacology Services, & Laboratories
Hybrid in Leeds
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Do you have a passion for scientific writing and clinical research?
Then, join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials.
Fortrea Clinical Pharmacology Services (CPS) supports the earliest and most critical phases of clinical development. Our teams work across project management, clinical operations, data, biometrics, laboratories, and scientific functions to deliver early‑phase and complex multi‑site studies for global sponsors.
From first‑in‑human studies to Phase 1B and exploratory programs, CPS generates the safety, tolerability, PK, and PD data that guide drug development decisions.
As a Medical Writer 1 you will play a key role mobilizing cross-functional teams in the development of essential clinical documents for early phase clinical trials (I-IIa), with a focus on safety and pharmacokinetics.
As one of the largest Clinical Research Organizations (CROs) in the world, we have four Early Phase Clinical Research Units (CRU) in the UK and US... and the jewel in the crown is our CRU at Drapers Yard Leeds. A brand new, world class, state-of-the-art 65,000 ft² Phase I clinic only 7 minutes walking from the train station.
This is a full-time, permanent job, ideal for candidates living in the Yorkshire area, as we offer a hybrid work model:
You will learn how to develop the documents that enable the conduct of a clinical trial and to analyze the data that will help the sponsor to decide the future of their molecule.
With on-the-job training and guidance from your colleagues and managers, by the end of your first year, success means you'll be able to:
This includes:
Project Manage the document development cycle from start to final deliverable
You´ll be the nexus where multiple teams´ expertise converge. You will coordinate and collaborate with multiple stakeholders, steer discussion, drive consensus and facilitate decision-making to propel the document development cycle forward:
Ideally, you'll also have experience working collaboratively across several teams and interacting directly with clients or external stakeholders. Some medical writing experience, particularly within a CRO, Pharma or Biotech environment, is ideal but not essential. If you're new to medical writing, we'll be looking for strong scientific writing, analytical skills and attention to detail developed through your professional experience or PhD.
To succeed in this job, you'll need to be proactive, adaptable and an excellent communicator. You'll be comfortable with changing priorities and requirements, and able to adjust your work as the needs of clients and project teams evolve.
Join Fortrea and be part of a team that values your skills and supports your career growth. Where do you see yourself?
Apply now and make an impact with Fortrea!
Learn more about our EEO & Accommodations request here.
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