Clinical Research Coordinator, UK

CLINICAL RESEARCH COORDINATORUK Site Network (Peterborough-Based)Assured Clinical Research Ltd | Full-Time | Ref: SW001Salary: Salary discussed at interview — please indicate your expectations.📍 Primarily based in Peterborough, Cambridgeshire | Travel across wider UK as needed as ACR expands Assured Clinical Research Ltd (ACR) is a growing independent clinical research organisation dedicated to expanding patient access to clinical trials within community and primary care settings across the UK. Working with sponsors, CROs, and healthcare partners, we deliver high-quality studies safely, ethically, and efficiently.We are looking for a motivated and organised Clinical Research Coordinator to join our UK site team. This is an exciting opportunity to be part of a dynamic, growing organisation at an early stage — with real scope to develop your clinical research career across a diverse and expanding study portfolio.This role is primarily based in Peterborough, Cambridgeshire, with occasional wider UK travel as ACR’s site network grows. The successful candidate will work closely with the Managing Director, UK, and Chief of Staff, providing operational support across assigned studies.THE ROLEWorking under the supervision of the Lead Chief of Staff and Principal Investigator, you will play a central role in the day-to-day delivery of clinical studies at ACR’s UK sites. Your responsibilities will span the full study lifecycle — from start-up through to close-out — ensuring participants receive an exceptional experience and that studies are conducted to the highest standards of quality and compliance.Key ResponsibilitiesCoordinate participant visits, scheduling, and follow-up activities across assigned research locationsSupport the informed consent process under delegation and supervision of the Principal InvestigatorPrepare, maintain, and review source documents and essential regulatory files (eReg/eCTMS)Perform data entry and query resolution in electronic data capture (EDC) systemsAssist with delegated clinical procedures, including clinical observations and biological sample collection, where appropriately trained and authorisedLiaise with investigators, sponsors, and CROs — including support during monitoring visits and site initiation activitiesManage study supplies, investigational product handling, and sample logistics in accordance with protocol requirementsHelp maintain regulatory, ethical, and GCP compliance across all assigned studiesDeputise for the Lead Clinical Research Coordinator in their absence, maintaining continuity of study operationsContribute to continuous process improvement and SOP development as ACR’s site network growsProvide operational support across new ACR research locations as the network expands across the UKABOUT YOUWe welcome applications from:Registered Nurses (NMC)Nursing Associates (NMC)Allied Health Professionals registered with the HCPCExperienced Clinical Research CoordinatorsOther healthcare professionals with relevant patient-facing experience and a genuine interest in clinical researchPrevious clinical research experience is essential.You will bring:A proactive, self-motivated approach with strong attention to detailExcellent organisational skills and the ability to manage multiple tasks or studies simultaneouslyConfidence working independently as well as collaboratively within a small, close-knit teamStrong written and verbal communication skills, with the ability to engage effectively with participants, healthcare professionals, investigators, and external partnersA compassionate, professional, and adaptable approach to patient-facing workConfidence with IT systems and willingness to learn clinical research software and electronic data capture platformsMotivation to contribute to a growing research organisation and develop your career in clinical researchREQUIREMENTSEssential2+ years experience in clinical research, including familiarity with clinical trials and day-to-day study operationsKnowledge of research protocols and the ability to follow and implement them accuratelyExperience with clinical trial documentation, data entry, and site coordination activitiesCurrent ICH-GCP certification (E6 R2 or R3), or willingness to undertake trainingFamiliarity with eCTMS, eReg, or EDC platformsRight to work in the United KingdomAbility to travel independently between research locations across Norfolk and occasionally elsewhere in the UKExcellent IT and communication skillsWHAT WE OFFERA competitive salary depending on experienceFull GCP training and ongoing professional development supportThe opportunity to join a growing independent research organisation at an exciting stage of its developmentA varied and stimulating role across a diverse clinical study portfolio spanning multiple therapeutic areasReal scope for career growth as ACR expands its UK site networkA collaborative, supportive team environment with a genuine focus on participant welfare and research quality READY TO MAKE RESEARCH ACCESSIBLE TO MORE PATIENTS?If you are passionate about delivering high-quality, patient-focused research in community settings and want to grow with an ambitious independent research organisation, we would love to hear from you.Assured Clinical Research Ltd is committed to promoting equality, diversity and inclusion. We welcome applications from all suitably qualified candidates regardless of age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, or sexual orientation.Information submitted as part of the recruitment process will be handled in accordance with UK data protection legislation and the Company’s Privacy Notice. Employment is subject to satisfactory references, verification of professional registration and right-to-work status, DBS clearance, and any other pre-employment checks required for the role.