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Discover International

Clinical Research Coordinator

United Kingdom
Posted about 21 hours ago
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Discover International Partnership Opportunity

Discover International is partnered with a UK-based CRO who are seeking a Clinical Research Coordinator to support multi-site clinical trials across oncology, cardiovascular, and rare disease indications.

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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Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.

P

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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It searches the market for you

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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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Strong

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.

Key Responsibilities

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  • Coordinate site start-up and maintain Trial Master Files (TMF) per ICH-GCP
  • Liaise with investigator sites, sponsors, and internal teams to hit trial milestones
  • Support CRAs with visit scheduling/reports and track patient recruitment
  • Prepare study materials (consent forms, CRFs) and manage study trackers
  • Help resolve data queries and ensure audit/inspection readiness
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Skills

Clinical Trial Coordination
Trial Master File (TMF) Management
ICH-GCP
Site Start-up
Patient Recruitment Tracking
Data Query Resolution
Audit Readiness
Case Report Forms (CRFs)
Informed Consent Forms
Stakeholder Liaison

Location

United Kingdom

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