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A prestigious university medical division in Oxford seeks a part-time Research Assistant to support vital cardiovascular research, collecting human tissue samples and data. Candidates should have a relevant degree and experience in clinical settings. Strong communication skills and attention to detail are essential, along with a proactive attitude towards research and patient care.
The closing date is 26 November 2025
An opportunity has arisen for a highly motivated, enthusiastic Science Graduate, Clinical Research Practitioner or Clinical Research Nurse to join a team of internationally recognised researchers contributing to the Cardiovascular Medicine Theme of the Oxford NIHR Biomedical Research Centre. The successful candidate will support patient‑oriented research that uses human tissue samples to explore the underlying mechanisms of heart disease.
The primary role will be to screen cardiac and vascular surgical lists for eligible patients, obtain informed consent, and collect and prepare human tissue and blood samples from patients undergoing elective cardiac or vascular surgery. Working across a small number of research groups, and in collaboration with Principal Investigators and research fellows, the postholder will focus on supporting studies involving the collection of human tissue samples that contribute to the world‑leading research of the BRC Cardiovascular Medicine Theme.
This is a part‑time appointment on a fixed‑term contract for 2 years. The post is funded by the NIHR Oxford Biomedical Research Centre (BRC), and the postholder will be based within a research nursing and support team at the Oxford Centre for Magnetic Resonance Research, within the Division of Cardiovascular Medicine at the John Radcliffe Hospital, Oxford (OX3 9DU).
The postholder must have a proactive, can‑do attitude, good organisational skills, excellent communication and interpersonal skills, as well as the ability to keep meticulous records. Specific training will be available. Administrative responsibilities will include inputting study data into an electronic database, complying with the regulatory framework of the Human Tissue Act (HTA), compiling annual reports, and attending team meetings.
Undertake safe, good quality, participant‑focused research in accordance with Good Clinical Practice (GCP) guidelines and the Research Governance Framework for Health and Care. Screen NHS patient records, recruit new participants, carry out the informed consent process, monitor and attend cardiac/vascular surgery lists, collect and process tissue and blood specimens, maintain high‑quality study data, attend multidisciplinary meetings, liaise with study personnel, and adhere to all local policies and standard operating procedures.
University of Oxford – Division of Cardiovascular Medicine