Hlx Life Sciences
French-speaking Clinical Research Associate

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Freelance CRA – UK | French & English Speaking
I’m currently supporting a CRO looking to bring an experienced Freelance CRA onto a part-time, sponsor-dedicated project.
The CRA will be based in the UK and work closely with both the CRO and sponsor teams, supporting sites as part of a global clinical trial. We’re particularly interested in CRAs who have experience working across international studies and ideally have previously supported sites in France.
Key responsibilities:
- Managing monitoring activities across assigned clinical trial sites
- Conducting site initiation, routine monitoring, and close-out visits
- Managing site relationships and acting as a key point of contact for investigators and site teams
- Monitoring recruitment, data quality, site performance, and key study metrics
- Identifying and escalating site-level risks and supporting resolution of study issues
- Ensuring compliance with the protocol, ICH-GCP, and applicable local regulations
- Reviewing source documentation, study documentation, and site files
- Supporting study start-up and site activation activities where required
- Completing monitoring reports and study documentation within agreed timelines
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.
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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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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.
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Experience required:
- Strong independent CRA and site monitoring experience
- Fluent in French and English
- UK based with the ability to travel for site visits when required
- Experience working on global/multinational clinical trials
- Previous experience monitoring or supporting clinical trial sites in France would be ideal
- Comfortable working across international and cross-functional study teams
- Strong knowledge of ICH-GCP and clinical trial regulations
- Oncology, Rare Disease, and/or Neurology experience preferred


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Contract details:
- Freelance / contract
- Part-time
- UK based
- Global clinical trial
- Site travel required
If you’re an experienced freelance CRA with French and English language skills and this sounds relevant to your background, please get in touch with your latest CV.
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