Job Title

Who are we?Clerkenwell Health is an innovative and leading Research Organisation specialising in the delivery of scientifically grounded Clinical Trials using its collaborative Contract Research Organisation (CRO), extensive Clinical Research Facility (CRF) Network, and leading Therapy Development Programme. Clerkenwell Health specialises in supporting the Mental Health and CNS (Central Nervous System) space, with a strong focus on psychedelic drug development.The RoleWere looking for a Study Coordinator to join our dynamic clinical operations team. Youll play a vital role in supporting the day-to-day conduct of clinical trials across our sites, ensuring high standards of compliance, patient care, and operational excellence.As a Study Coordinator, you'll work closely with Principal Investigators, clinical staff, and sponsors to facilitate all aspects of clinical research from feasibility to closeout. Your expertise will help ensure trials are conducted according to ICH-GCP, MHRA, and Clerkenwells internal SOPs, supporting meaningful innovations in mental health care.What will the role entail?Collaborating with the PI and site leads to support the design, delivery, and management of clinical trialsReviewing protocols and ensuring site readiness through study start-up, including regulatory submissions and training coordinationCoordinating and managing study documentation including the TMF/ISF, CRFs, consent forms, and source documentationAssisting with participant screening, enrolment, and ongoing study visit schedulingEnsuring data integrity and timely completion of case report formsSupporting trial monitoring and audit activities and helping implement findings and CAPAsEngaging with external vendors and regulatory bodies as neededManaging study closeout activities and secure archiving of clinical trial materialsParticipating in and completing all required training, both internal and sponsor-ledUpholding Clerkenwells values and ensuring the safety and wellbeing of trial participantsWhat will you need to succeed?Degree in a science or health-related discipline (or equivalent experience)Demonstrated experience in clinical research or clinical trial administrationSound understanding of ICH-GCP guidelines and clinical governanceExcellent organisational skills and attention to detailStrong communication and interpersonal skillsProficiency in Microsoft Office and clinical trial management systemsA proactive, self-motivated attitude and a team-oriented approachExperience in CNS or mental health trials is desirable but not essentialInterview ProcessThere will be an initial screening call with the recruiter, followed by a 2-stage interview process with the clinical operations team and site leadership.Is this the role for you?At Clerkenwell Health, our core values are Compassion, Collaboration, Innovation, and Integrity. If you're excited about playing a key role in advancing psychedelic and mental health research and feel aligned with our mission and valueswed love to hear from you!Best of luck