At a Glance
- Tasks: Monitor exciting Phase I–Ib clinical trials and collaborate with top-notch teams.
- Company: Fortrea Clinical Pharmacology Services, a leader in early clinical development.
- Benefits: Competitive salary, flexible working, and access to innovative trial technology.
- Other info: Join a global team in a modern Leeds facility with great career growth.
- Why this job: Experience real-time clinical trials and make a difference in life-saving medicine.
- Qualifications: Experience in clinical research or related roles; life science degree preferred.
The predicted salary is between 37000 - 44000 £ per year.
Have you ever wanted to see a clinical trial happen in real time? This is not monitoring from a distance. At Fortrea Clinical Pharmacology Services in Leeds, CRAs are on site, in the flow of the study, when it matters most. You see dosing days. You walk the clinic floor. You review data as it is generated, not months later. It is a different way to work as a CRA. It all happens inside a world‑class 100-bed, 65,000 ft² Clinical Research Unit, only 7 minutes from the train station, where life‑saving medicines begin their journey.
We are currently hiring CRA I and CRA II to support Phase I–Ib studies. These are full‑time, permanent positions. Ideally, you live in Yorkshire or within driving distance of our Drapers Yard clinic.
Why a career in early clinical development at Fortrea? Involved in studies even before they are won (i.e., participating at BID meetings), you will be on-site for the moments sponsors travel the world to witness. This includes first‑in‑human dosing days, when you review eligibility, observe dosing and safety procedures in real time, and see decisions unfold as the study begins. You will also follow PK samples into the lab, and work side by side with clinic, pharmacy, and lab teams during the most critical moments of the study. Rarely work alone. Studies are often monitored alongside another CRA, and during busy periods you will find several colleagues on site at the same time. The Leeds Clinical Research Unit gives you the option to work from the office, collaborate face to face, and build real working relationships with CRAs, CTLs, and clinical teams. You will be part of a global team, closely interacting with the other Fortrea’s clinics in the US.
Modern systems. Higher‑value CRA work Our clinical systems are built for modern monitoring. Integrated eSource and EDC reduce mechanical SDV and allow CRAs to focus on data integrity, protocol compliance, and study quality. The result is higher‑value work, closer to science, and with less administrative burden.
What you will do:
- Monitor Phase I–Ib studies across Fortrea CRU and selected UK sites.
- Perform Process Monitoring, Site Initiation, Routine Monitoring, and Close‑out visits.
- Review source data, protocol compliance, and data quality using modern eSource and EDC systems.
- Collaborate closely with clinical, lab, and project teams during fast‑paced study timelines.
Who we are looking for:
- CRA I: minimum 6 months of experience in clinical research or site‑based roles such as research nurse, in‑house CRA, site coordinator or similar. Clinical research unit experience (e.g. research technician, data monitors) considered.
- CRA II: minimum 2 years independent clinical monitoring experience. A life science degree or nursing qualification. You must be independently eligible to work in the UK.
What we offer:
- Salary aligned to level plus car allowance.
- Flexible working arrangements.
- Exposure to early‑phase science that accelerates CRA development.
- A global collaborative team environment based in a modern Leeds CRU.
- Access to innovative clinical trials technology.
Join Fortrea and be part of the stage where medicines are proven safe for the first time.
Clinical Research Associate II Leeds employer: Fortrea
At Fortrea Clinical Pharmacology Services in Leeds, we pride ourselves on being an exceptional employer that offers a unique opportunity for Clinical Research Associates to engage directly in the heart of clinical trials. Our world-class facility fosters a collaborative work culture, where you can build meaningful relationships with colleagues and gain invaluable exposure to early-phase science, all while enjoying flexible working arrangements and competitive benefits. Join us to be part of a global team dedicated to advancing life-saving medicines in a supportive and innovative environment.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II Leeds
✨Tip Number 1
Get to know the company inside out! Research Fortrea and their clinical trials, so you can chat about their work during interviews. This shows you're genuinely interested and ready to jump in.
✨Tip Number 2
Network like a pro! Connect with current CRAs or team members on LinkedIn. Ask them about their experiences and any tips they might have. It’s a great way to get insider info and maybe even a referral!
✨Tip Number 3
Prepare for those tricky interview questions! Think about your past experiences and how they relate to the CRA role. Use the STAR method (Situation, Task, Action, Result) to structure your answers and impress the interviewers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the Fortrea team.
We think you need these skills to ace Clinical Research Associate II Leeds
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight relevant experience, especially in clinical research or site-based roles. We want to see how your background aligns with what we do at Fortrea!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about early clinical development and how you can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Team Spirit:Since collaboration is key at Fortrea, make sure to highlight any experiences where you've worked closely with others. Whether it's in a clinical setting or another team environment, we want to know how you thrive in a group!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Fortrea
✨Know Your Clinical Trials
Familiarise yourself with the basics of clinical trials, especially Phase I–Ib studies. Understand the significance of first-in-human dosing days and be ready to discuss how you can contribute to monitoring and ensuring data integrity in real-time.
✨Showcase Your Experience
Be prepared to highlight your relevant experience, whether it's from previous CRA roles or site-based positions. Use specific examples to demonstrate your understanding of protocol compliance and data quality, as these are crucial for the role.
✨Emphasise Team Collaboration
Since this role involves working closely with various teams, emphasise your ability to collaborate effectively. Share examples of how you've worked alongside clinical, lab, and project teams in fast-paced environments to achieve common goals.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical research and the technologies they use. This shows your genuine interest in the role and helps you understand how you can fit into their innovative environment.
