Barrington James
CLINICAL RESEARCH ASSOCIATE (CRA)

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London, UK (Hybrid) Full Time, Permanent
We are looking for a motivated Clinical Research Associate (CRA) who is detail oriented to join a growing research team. This hybrid role requires the candidate to monitor clinical trial sites within a reduced travel area in London and maintain close engagement with investigative sites. The successful candidate will ensure that all clinical studies are conducted in line with ICH-GCP, applicable regulations, study protocols and sponsor requirements. You will have to work well together with investigators, staff, and internal project teams to support the successful delivery of clinical trials.
Key Responsibilities
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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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.
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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.
- Make sure the clinical trial data is accurate, complete and integral.
- Protocol deviations and outstanding site issues must be identified, documented and checked up on.
- Build and maintain strong working relationships with the site personnel and investigators.
- Support site training and provide constant guidance throughout the study life cycle.
- Prepare monitoring reports and sustain essential trial documentation.
- To ensure study milestones are completed, the candidate will need to work with Clinical Trial Managers and cross-functioned teams.
- Help support regulatory audits and inspection readiness where required.
- Maintain accurate tracking of site performance and recruitment.


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Essential Requirements
- Bachelor’s degree in Life Sciences
- Minimum 2 years’ experience working as Clinical Research associate in clinical research
- Strong organisational skills with exceptional attention to detail
- Full right to work in the UK
Desirable
- Having experience in multiple therapeutic areas.
- Experience in working in a CRO, sponsor or academic clinical research environment.
What we offer
- Competitive salary
- Opportunities for career progression.
- Pension scheme and annual leave entitlement.
Working Pattern
- Hybrid Work
- All sites within London.
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