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.
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
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.
- 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.
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What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
