Clinical Research Coordinator

Location: On-site, PeterboroughEmployment Type: Full-timeOverviewWe are supporting a growing clinical research site network seeking a Clinical Research Coordinator to support the day-to-day delivery of clinical trials at our Peterborough site. This is a hands-on, on-site role working closely with investigators, patients, and sponsors to ensure studies are run to GCP and protocol.Key ResponsibilitiesCoordinate and support clinical trials from start-up to close-outScreen, recruit, and schedule study participantsConduct study visits and collect trial data in line with protocolMaintain accurate study documentation and trial master filesLiaise with investigators, sponsors, CROs, and monitorsEnsure compliance with GCP, SOPs, and regulatory requirementsSupport monitoring visits, audits, and inspectionsRequirementsExperience working in clinical research (site-level experience preferred)Good understanding of GCP and clinical trial processesStrong organisational and communication skillsComfortable working on-site in a fast-growing environmentDesirablePrevious experience as a Clinical Research Coordinator or Research NurseExperience working across multiple studies or therapeutic areas

Created: 2026-01-19