🚀 Clinical Research Coordinator

Clinical Research Coordinator (Part-Time) – Global CRO Client | Torpoint, Cornwall 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.