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.