Clinical Research Facilitator - Fixed Term
| Dyddiad hysbysebu: | 28 Ionawr 2026 |
|---|---|
| Cyflog: | £38,880.00 i £46,819.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £38880.00 - £46819.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 10 Chwefror 2026 |
| Lleoliad: | Holgate, YO26 4GG |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | B0260-26-0014 |
Crynodeb
Job Summary: We are seeking a part time Clinical Research Facilitator who is genuinely motivated to make a difference in healthcare, who values collaboration, curiosity and continuous improvement, and who wants to be part of an organisation where people, wellbeing and quality of care truly come first. This role will be fixed term for 12 months. This is an opportunity to play a meaningful role in shaping and supporting the future of clinical research at Nimbuscare. We are seeking an individual who is motivated by purpose and inspired by innovation, and who wants to contribute to making research more patient-centred, inclusive and efficient. Main Duties and Responsibilities: Clinical Trial Coordination Coordinate and manage all aspects of assigned clinical trials from site initiation to close-out. Conduct study visits, including obtaining informed consent, performing protocol-required procedures, and collecting source data using eSource systems. Ensure timely and accurate entry of study data into electronic case report forms (eCRFs). Technology & Documentation Utilise eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory-compliant study records. Support site readiness and compliance with 21 CFR Part 11, ICH GCP, and sponsor SOPs. Regulatory Compliance Maintain up-to-date regulatory documents and study binders (electronic and/or paper as required). Assist with preparation for sponsor, CRO, or regulatory audits. Patient Engagement & Safety Recruit, screen, and enrol study participants according to protocol inclusion/exclusion criteria. Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol. Collaboration & Support Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff. Support training and mentoring of new research staff as assigned. Provide on-site support at additional study locations when required (occasional travel). Support staff education and understanding of research, and quality processes. Occasional travel may be required for site visits, team meetings or training events Other: The job description is provided as an outline of the key tasks and responsibilities and is not intended to be an exhaustive list. The job will evolve over time to reflect the changing needs of Nimbuscare and its services as well as the personal development of the post holder.