Research Nurse/Clinical Trials Practitioner
Lymphoma Trials Team
Band 6
12‑month fixed term contract
The Research Nurse/Clinical Trials Practitioner is an autonomous specialist working within the multi‑disciplinary team. The post holder will take responsibility for the co‑ordination and management of a clinical research portfolio comprising in‑house, national and international phase II and III clinical trials in haematological malignancies.
Responsibilities
- Educate patients and colleagues; coordinate care of patients on trials; collect and prepare biological samples; collect trial data; monitor drug side effects and treatment modalities.
- Enable patients to make informed choices by providing advice, information and acting as patient advocate.
- Support research in all oncology and haematological malignancies; provide cross‑cover for team members.
- Coordinate and conduct in‑house and national/international phase I, II and III trials.
- Submit new trials for ethics and R&D approval.
- Create and maintain trial site files and protocol files.
- Document trial data according to ICH GCP guidelines.
- Appraise research protocols; assist in database development.
- Collaborate with multidisciplinary team to assess, plan, implement and evaluate clinical research protocols.
- Consult with primary investigators, research organisations and industry to develop and deliver protocols.
- Understand pre‑clinical data and rationale for testing investigational agents.
- Ensure case report forms are completed per ICH GCP within appropriate time.
This role is open only to qualified clinical nurses with a passion for research.
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