Clinical Research Coordinator (Part-Time) – Global CRO Client | Torpoint, Cornwall
A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully.
Location: Torpoint, Cornwall
Hours: Part-time, 24 hours per week
Contract: 12-month contract
Pay Rate: £20–25 per hour
Start Date: ASAP
About the Role
We are partnering with a leading global Contract Research Organisation (CRO) to recruit an experienced and detail-oriented Clinical Research Coordinator (CRC) for an exciting part-time position based in Torpoint, Cornwall.
This is an excellent opportunity to contribute to high-quality clinical research within a respected global organization, supporting investigators and site teams in the delivery of pivotal studies that drive medical progress.
Key Responsibilities
* Coordinate day-to-day clinical trial operations in accordance with ICH-GCP, study protocols, and site SOPs.
* Schedule subject visits, manage patient study calendars, and send appointment reminders.
* Assist with patient prescreening, recruitment, and the informed consent process.
* Enter and verify study data in Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS), ensuring accuracy and completeness.
* Maintain organized and compliant trial documentation, including regulatory and ethics submissions.
* Track study progress, resolve data queries, and support clear communication between site staff, monitors, and sponsors.
Candidate Requirements
* Minimum 1 year of experience as a Clinical Research Coordinator, Research Assistant, or in a similar research support role
* Working knowledge of clinical trial operations, regulatory standards, and GCP guidelines.
* Strong attention to detail, organizational, and multitasking abilities.
* Proficiency with Microsoft Office; experience with EDC or CTMS systems is advantageous.
* Excellent interpersonal and communication skills, with a patient-focused and proactive approach.
* Background in life sciences, pharmacy, nursing, or biomedical research preferred.
Why Apply?
* Join a globally recognised CRO known for innovation and clinical excellence.
* Gain valuable hands-on experience across multiple therapeutic areas.
* Flexible part-time schedule and supportive team environment.
* Opportunity to make a direct impact on the success of vital clinical studies.