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We are looking for a Clinical Research Coordinator to recruit, consent and schedule trial participants. You will collect and enter study data accurately, and support investigators with regulatory and ethics submissions. Required: hands-on experience with Patient recruitment, Informed consent, Visit scheduling, Case report forms, and working knowledge of EDC systems, CTMS, Excel. Preferred: GCP Certification or BSc Life Sciences. Success in this role is measured by enrolment against target, data query rate, protocol deviations.