Clinical Research Coordinator
- Own the day-to-day running of studies: from study start-up to site close-out, you’ll keep everything moving.
- Chase down ethics approvals, track regulatory documents, and make sure submissions don’t get stuck.
- Be the go-to for sites - solving problems, escalating as needed, and keeping everything on track.
- Monitor performance, flag issues early, and follow up relentlessly until they’re fixed.
- Coordinate vendors and supplies meticulously - you will always know what is needed, where it is needed and who needs it by when
- Build the tools and trackers that keep us lean, fast, and compliant.
- Jump in where needed to help write SOPs, prep materials, and support CRF training sessions.
- Get the right information to the right people, at the right time - no ambiguity - trusted and simple communication.
- 1+ years of experience in clinical research, preferably in medical devices or diagnostics.
- Strong knowledge of GCP, ISO 14155, and ethics/regulatory submission processes in the UK.
- Highly organised, detail-oriented, and proactive - you spot issues before they become problems.
- Seeks satisfaction by completing tasks and reaching milestones.
- Strong communication and collaboration skills; you're comfortable working across teams and with sites.
- Confident using digital tools and trial management systems - and quick to learn new ones.
- Experience working in early-stage or rapidly scaling companies.
- Familiarity with FDA regulations and running trials in the US - or anywhere outside of the UK.
- A background in science, engineering, or regulatory affairs.
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