Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR – PHASE I





THE OPPORTUNITY

Ready to take your clinical research career deeper into Phase I?

Join a leading early-phase research site delivering first-in-human, SAD/MAD and dose-escalation studies, working directly with Investigators, Sponsors and CROs.

You'll play a hands-on role in participant screening, dosing, safety assessments, PK/PD sampling, study visits and clinical documentation — making a direct impact on bringing new therapies into development.





WHAT YOU'LL DO


- Coordinate Phase I studies from start-up through close-out.
- Manage participant screening, enrolment, dosing and follow-up.
- Support SAD/MAD, dose-escalation and FIH studies.
- Coordinate vital signs, ECGs, labs, PK/PD sampling and safety assessments.
- Monitor and document AEs, SAEs and protocol deviations.
- Maintain accurate source documentation and EDC/eCRF data.
- Work closely with Investigators, Sponsors, CROs and clinical teams.
- Support monitoring visits, audits and inspections.






WHAT YOU'LL BRING


- 2+ years' clinical research experience.
- Direct Phase I experience is essential.
- Experience in a Phase I unit, early-phase site or SMO.
- Strong understanding of ICH-GCP and FDA requirements.
- Experience with participant screening, dosing and safety assessments.
- Excellent organisation, attention to detail and communication skills.