Interim Clinical Research Assistant Practitioner
| Company: | NHS Jobs |
|---|---|
| Salary: | Negotiable |
| Hours: | Full-time |
| Location: | Sandbach, CW11 1EQ |
| Job type: | Contract |
| Posting date: | 8 Sept 2026 |
| Closing date: | 20 Sept 2026 |
Summary
Clinical Duties Undertake venipuncture in accordance with study protocols, infection prevention and control standards, and local policy. Perform and accurately record ECGs. Process biological samples safely and competently, including the operation of a centrifuge. Label, prepare, and dispatch specimens in line with study requirements and laboratory guidance. Prepare clinical areas and equipment for research visits, ensuring cleanliness and readiness. Support research clinics and participant appointments as required. Extra physical assessments may be required for specific studies, but full training will be given as per study protocol. Research Coordination and Administrative Duties Provide administrative support for the team which will includes duties such as filing, printing, appointment booking and answering patient calls. Support the team with study specific administrative tasks such as managing courier collections, lab kit ordering, lab kit preparation. Assist in the coordination, implementation, and rollout of research projects within the practice. Identify and screen potential participants using clinical IT systems and approved search tools. Maintain accurate and contemporaneous research documentation in accordance with study protocols. Complete data entry onto electronic case report forms and research databases. Manage study-related correspondence, appointment booking, and participant follow-up. Liaise with external research teams, sponsors, and research network staff as required. Ensure secure storage, archiving, and maintenance of study files. Managing samples collections using dry ice. IT and Data Responsibilities Confidently utilise electronic clinical systems for patient searches, coding, and data extraction. Maintain high standards of data quality and confidentiality in line with GDPR and NHS data governance requirements. Support digital reporting and research performance monitoring. Assist with audits and data validation exercises. Governance and Professional Responsibilities Work within the scope of competence and under the supervision of the Research Lead / team Adhere to Good Clinical Practice (GCP) and all relevant research governance frameworks. Participate in mandatory training and maintain required clinical competencies. Complete all study protocol specific training in a timely manner Contribute to incident reporting, significant event reviews, and quality improvement initiatives. Maintain patient confidentiality and uphold professional standards at all times.