Clinical Trial Coordinator

Clinical Research Coordinator Location: Warwickshire Working Pattern: Onsite Contract length: Short term contract with possibility of extension About the Role An exciting opportunity has become available for a Clinical Research Coordinator to support the delivery of innovative clinical studies. This position is ideal for someone with previous clinical research experience who enjoys working in a fast-paced environment and wants to play a key role in the successful execution of clinical trials. Responsibilities Coordinate day-to-day clinical trial activities from study start-up through to close-out. Support participant recruitment, screening and enrolment activities. Schedule study visits and maintain accurate study documentation. Ensure all study files are maintained in accordance with GCP and regulatory requirements. Collect, review and enter study data while ensuring quality and accuracy. Support monitoring visits, audits and inspections. Assist with regulatory submissions and essential document management. Act as a key contact between participants, investigators, sponsors and study vendors. Track study progress and assist with milestone delivery. Requirements Previous experience as a Clinical Research Coordinator, Clinical Trial Coordinator, Study Coordinator, Research Nurse or similar clinical research role. Good understanding of ICH-GCP guidelines and clinical trial processes. Experience working with study documentation and data collection activities. Excellent organisational and communication skills. Ability to manage multiple priorities and work to deadlines. Degree in Life Sciences, Nursing, Pharmacy, Biomedical Science or a related discipline is advantageous.