Dewislen

Clinical Trial Research Nurse

Manylion swydd
Dyddiad hysbysebu: 08 Awst 2025
Cyflog: £46,419.00 i £55,046.00 bob blwyddyn
Gwybodaeth ychwanegol am y cyflog: £46419.00 - £55046.00 a year
Oriau: Llawn Amser
Dyddiad cau: 21 Awst 2025
Lleoliad: London, EC1A 7BE
Cwmni: NHS Jobs
Math o swydd: Cytundeb
Cyfeirnod swydd: C9259-25-1810

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Crynodeb

An exciting opportunity has arisen for a Clinical Trial Research Nurse to work as part of the Cancer Research Delivery Group (CRDG) and Public-Patient Involvement & Engagement (PPIE) team. The Centre is: Generously funded by a joint initiative between the Department of Health and Cancer Research UK Part of a nationwide network of 18 centres of scientific and clinical excellence Aims to drive new anti-cancer treatments to patients Affiliated with the National Cancer Research Network and thus incorporates Phase 1 through to Phase 4 clinical trials In bringing together laboratory and clinical patient-based research, our Centre promotes the translational work needed to develop new anti-cancer drugs and diagnostics from the laboratory into clinics and then to test them in early phase clinical trials. The PPIE group is a diverse, proactive, and dynamic group of patients, relatives, and members of the public with a strong interest in cancer research. The group supports researchers at every stagefrom grant applications and service development to reviewing patient-facing research materials. Involving patients and the public in research is not just beneficialits essential. Their perspectives ensure that studies address real patient needs, improve health outcomes, and make findings more accessible to the communities we serve. Given our diverse and often underserved community, we prioritise equity, diversity, and inclusion (EDI) in all our work. We actively collaborate with other research centres, engage with local communities, and organise research awareness events to promote participation in studies and improve access to research opportunities. The Clinical Trials Research Nurse will also support the CECM CRDG portfolio of clinical trials to improve patient recruitment and ensure accurate and timely completion of trial data and documentation. Duties will include identifying potential patients to participate in trials, coordinating trials as per study protocols, collection of clinical data on Case Report Forms (CRFs), and following the principles of Good Clinical Practice (GCP). In addition, the post holder will take a leading role in the Centres PPIE activities, working with our PPIE group and external groups to continue and grow the activities. The successful candidate will have experience of working in an oncology / haematology nursing environment and it would be useful to have chemotherapy training. You must have a good understanding of Good Clinical Practice (GCP) and the regulatory environment that surrounds clinical research and it would be advantageous if you have some experience in clinical research. Experience of working with PPIE teams would also be beneficial. Although this position is a 12 months fixed-term contract, the actual contract duration will be adjusted to account for the time taken to advertise the post, complete the hiring process, and finalise pre-employment checks. This means the contract will begin when the candidate starts the role and may be slightly shorter than 12 months. The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below.

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