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- 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, car allowance, and exposure to innovative science.
- Other info: Join a global team in a modern, collaborative environment in Leeds.
- Why this job: Experience real-time clinical trials and make a difference in life-saving medicine.
- Qualifications: Life science degree or nursing qualification; CRA experience preferred.
The predicted salary is between 37000 - 45000 £ 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.
- 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 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
We are hiring at two experience levels:
- CRA I: minimum 6 months’ experience in clinical research or site-based roles such as research nurse, in-house CRA, site coordinator or similar. We will also consider Clinical Research Unit experience (e.g. Research Technician, Data Monitors, etc.).
- 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
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II Leeds
✨Tip Number 1
Get to know the company! Research Fortrea and understand their mission and values. This will help you tailor your conversations during interviews and show that you're genuinely interested in being part of their team.
✨Tip Number 2
Network like a pro! Connect with current or former employees on LinkedIn. Ask them about their experiences and any tips they might have for landing a role as a CRA at Fortrea. Personal connections can make a huge difference!
✨Tip Number 3
Prepare for the interview by practising common CRA scenarios. Think about how you'd handle real-time data review or collaboration with clinical teams. Being ready to discuss these situations will set you apart from other candidates.
✨Tip Number 4
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 Fortrea and being part of their innovative clinical research 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, and don’t forget to mention any specific skills that align with what we’re looking for!
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 your background makes you a great fit for our team at Fortrea. Keep it engaging and personal!
Showcase Your Team Spirit: Since we value collaboration, make sure to highlight any experiences where you’ve worked closely with others. Whether it’s in a clinical setting or during your studies, showing that you can work well in a team will definitely catch our eye.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the details you need about the role right there!
How to prepare for a job interview at Fortrea
✨Know Your Clinical Trials
Familiarise yourself with the latest trends in clinical research, especially Phase I–Ib studies. Understand the significance of first-in-human dosing days and be ready to discuss how you can contribute to the real-time monitoring process.
✨Showcase Your Team Spirit
Since collaboration is key at Fortrea, prepare examples that highlight your experience working in teams. Be ready to share how you've successfully collaborated with clinical, lab, or project teams in past roles.
✨Master the Modern Systems
Brush up on your knowledge of integrated eSource and EDC systems. Be prepared to discuss how these tools enhance data integrity and protocol compliance, and how you’ve used similar technologies in your previous roles.
✨Ask Insightful Questions
Prepare thoughtful questions about the role and the company culture. Inquire about the specific challenges faced during early-phase studies and how the team collaborates to overcome them. This shows your genuine interest in the position and the organisation.