Please refer to the attached job description and person specification for full details of responsibilities.
Working under supervision to identify potential participants from the Trusts clinical services, community services, university and NHS databases, specialist clinics, third sector organisations, schools and other access routes, for RDN portfolio and non-portfolio studies and clinical trials.
Prepare for and support research study visits, ensuring clinical areas, equipment, and documentation are ready and compliant with study requirements.
Undertake phlebotomy and assist with the collection, labelling, processing, and shipment of biological samples in accordance with study and relevant SOPs.
Perform delegated clinical tasks such as measuring vital signs, ECG recording, height/weight measurements, and other protocolspecific assessments once trained and deemed competent.
To maintain accurate patient records and ensure all relevant information is documented within the patients medical notes and study source documentation.




Supporting the study lead with the preparation for the monitoring visit ensuring the Investigator Site File (ISF) or Trial Master File (TMF) sections are up to date.
Maintain qualified awareness of subject area, including up to date understanding of all relevant legislation, Trust policies, procedures and guidelines.
Monitor participants during and after study procedures, promptly escalating any concerns about patient safety or wellbeing to the supervising nurse or clinical team.
Contribute to maintaining a safe clinical environment, including infection control, equipment checks, and adherence to local health and safety policies.
Accompany the participant to the study related procedures, i.e. imaging department and assist with checkin.
Cambridgeshire and Peterborough NHS Foundation Trust
Cambridge University Hospitals NHS Foundation Trust
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📌 Clinical Research Technician (Western Australia)
🏢 Allscreens Nationwide
📍 Western Australia