Fortrea
Medical Writer I Yorkshire

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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)
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.
LOCATION
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:
- Initially, 3 days’ office presence in Leeds for training and teamwork is needed.
- Rest of the week, you could work remote.
WHAT YOU WILL DO
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.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
See breakdownIt searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Learn the science behind Medical Writing
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:
- Drive the development of simple design Protocols and Clinical Study Reports (CSRs) with minimal supervision.
- Navigate the fast-paced timeliness of the document development cycle.
This includes:
- Critically reviewing and interpreting clinical research data (particularly Pharmacokinetics and Safety).
- Condensing data and conclusions into clear concise language in Protocols and CSRs.
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:
- Ensuring alignment with sponsor goals and project milestones while monitoring study progress.
- Fostering regular communication with subject matter experts (SMEs) to streamline document development (getting inputs timely, consolidating contributions or answering questions.)
Manage client interaction
- Setting client expectations with document development.
- Addressing feedback and confidently leading meetings with Big Pharma and Biotech clients.


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WHO YOU ARE
- Bachelor's degree in biomedical, life sciences, or related discipline.
- Some medical writing experience within a CRO, Pharma, or Biotech is ideal.
- If you don't have medical writing experience, we still want to hear from you if you have strong scientific writing, data analysis and attention to detail gained from, i.e.:
- Recently completing your PhD, or
- Working in a fast-paced research lab, handling experimental data analysis and results report writing.
To succeed in this job, you’ll need visibility, proactivity and excellent communication skills. You should be comfortable with changing priorities and deadlines, managing complex regulatory documents, and confidently engaging with experts in their medical and statistical fields.
WHY FORTREA?
- Diverse Career Path: Unique training schemes and opportunities to shape your career path.
- Supportive Environment: Comprehensive training, management support, and a network of SMEs to help you thrive.
- Career Growth: Whether you're passionate about scientific writing or aspire to leadership roles, your journey with us is driven by your aspirations.
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!
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