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Cpl

Clinical Research Associate

England
£55k – £65k/yr
Posted about 16 hours ago
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CRA II / Senior Clinical Research Associate – French Speaking

Location: UK-based / Remote
Travel: UK-wide, plus France & French-speaking Belgium.
Site visits: 7-8 visits per month
Contract: Permanent, Full-time
Focus: Phase II/III Clinical Trials | Oncology / Rare Disease
Salary: £55,000-£65,000 (Flexible on experience)

CPL Life Science are currently supporting a specialist CRO in the search for an experienced CRA II / Senior CRA to join their Clinical Monitoring team.

This is an excellent opportunity for a CRA with strong Phase II/III monitoring experience who is fluent in English and French and enjoys working across complex clinical trials and international sites.

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

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your 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.

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Strong

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.

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Key Experience

  • Extensive on-site clinical monitoring experience across Phase II and Phase III clinical trials
  • Proven experience conducting Pre-Study, Site Initiation, Interim Monitoring and Close-Out Visits
  • Strong understanding of site qualification, selection and ongoing site oversight
  • Experience assessing investigator sites, including staff, facilities, equipment, resources and study capability
  • Confident in providing site staff training and supporting sites throughout the study lifecycle
  • Experience identifying, documenting and resolving site issues, protocol deviations and compliance concerns
  • Ideally, previous experience working on complex clinical trials, particularly oncology and/or rare disease
  • Strong understanding of GCP, clinical trial processes and regulatory requirements
  • Excellent communication, collaboration and problem-solving skills

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Strong experience in Oncology trials is essential, as well as fluent French.

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Skills

Clinical Monitoring
Phase II Clinical Trials
Phase III Clinical Trials
Oncology
Rare Disease
GCP
Site Qualification
Site Initiation Visits
Interim Monitoring Visits
Close-Out Visits
French Fluency
English Fluency
Regulatory Compliance
Site Staff Training
Problem Solving
Collaboration

Location

England, United Kingdom

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