Clinical Trial Study Coordinator

Study Coordinator (Temporary Cover with a possibility of extension upon review)Bioluminux Clinical Research – Milton KeynesContract: Temporary (duration to be confirmed)Bioluminux Clinical Research is an integrated research organisation conducting industry-sponsored clinical trials across the UK. We are seeking an experienced Study Coordinator to provide temporary cover within our Milton Keynes site team.Key ResponsibilitiesCoordinate daily clinical trial activities in line with GCP, protocol, and sponsor requirements.Support Investigators and site staff with participant visits, data collection, and sample handling.Ensure timely and accurate data entry into eCRFs and maintenance of essential documents.Communicate effectively with sponsors, monitors, and vendors to ensure smooth study delivery.Maintain source documentation and regulatory files to audit-ready standards.Essential RequirementsDegree in Medicine, Nursing, Pharmacy or Health Sciences (e.g., MBBS, BSc Nursing, Biomedical Science, Pharmacy, or related field).At least 6 months of experience working on industry-sponsored clinical trials (Phase II–IV preferred).Strong understanding of ICH-GCP and clinical research site operations.Excellent organisation, attention to detail, and communication skills.Ability to manage workload independently while working within a multidisciplinary team.Right to work in the UKDesirableExperience with electronic systems (eCRF, CTMS, eTMF).Previous involvement in respiratory, metabolic, or vaccine trials.Previous patient-facing roles in NHS or private healthcareCertification in Clinical Research CoordinationSalary: £31,000 per annum (pro rata)This is an excellent opportunity to contribute to a growing, patient-focused research organisation known for its quality and innovation.To apply: Please send your CV and a brief cover letter to careers@bioluminux.comwith the subject line “Study Coordinator – [Your Name]”.