Job Title

Who we are Clerkenwell Health is an innovative and leading research organisation specialising in the delivery of scientifically grounded clinical trials. Through our collaborative CRO model, extensive site network, and pioneering Therapy Development Programme, we support research in Mental Health and Central Nervous System (CNS) disorders - with a strong focus on psychedelic drug development. The Role Were seeking a Study Coordinator to join our growing clinical research team. Youll play a vital part in ensuring the smooth and compliant delivery of Phase 13 clinical studies, working across site activities, laboratory processes, and participant coordination. This is a hands-on and dynamic position where no two days are the same. Youll be central to the planning and running of studies - ensuring timelines are met, data is accurate, and participants receive the highest standard of care. Key Responsibilities Oversee the day-to-day coordination of studies across Clerkenwell Healths clinical and laboratory sites Support study start-up, ongoing delivery, and closeout in line with protocol and regulatory requirements Assist with investigational product management under the supervision of the site pharmacist Provide direct support to participants - greeting them onsite, facilitating study visits, explaining procedures, and ensuring comfort and safety Coordinate sample collection, labelling, storage, and transfer according to study protocols Support the preparation and maintenance of study documentation, trackers, and logs Contribute to feasibility assessments, documentation development, and risk evaluation activities Maintain inspection readiness and support audits and monitoring visits Manage data entry and quality control to ensure accuracy and compliance with ICH-GCP standards Act as a point of contact between study teams, sponsors, and internal departments to resolve logistical or procedural queries Support team training, onboarding, and general site coordination Assist with study-related financial tracking, invoicing, and documentation management What Youll Bring Degree in a scientific or health-related discipline Prior experience within clinical research or healthcare Proficiency in Microsoft Office and/or electronic data systems Eligibility to work in the UK Experience in laboratory or pharmacy support within a research environment Familiarity with GCP, GMP, GDPR, and related regulatory frameworks Why Join Us At Clerkenwell Health, we combine compassion, scientific rigour, and innovation to advance mental health research. As a Study Coordinator, youll play a key role in shaping the future of clinical trials, contributing to life-changing studies in an inspiring and supportive team environment.55b20050-bc17-4e5d-bfce-3c406318dffc