Clinical Research Coordinator
1 day ago
Torpoint
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.