Clinical Research Portfolio Coordinator
1 week ago
Job Overview
The Clinical Trials Practitioner is an autonomous specialist working within a multi-disciplinary team to coordinate and manage clinical research portfolios comprising in-house, national, and international phase I, II, and III trials. Responsibilities include education of patients and colleagues, coordination of care for patients on trials, collection and preparation of biological samples, collection of trial data, and monitoring of side effects.
Main Duties
- Support the running of clinical trials across paediatric and teenage/young adult portfolios as per GCP guidelines.
- Collaborate with research team members, including research nurses, clinical trial practitioners, and data managers.
- Provide expertise in assessing, planning, implementing, and evaluating clinical trial protocols within the MDT.
- Evaluate patient eligibility and ensure pre-study tests are undertaken and reviewed.
- Act as patient advocate and assist in obtaining informed consent.
- Register and randomise patients, provide general information to patients and families, and document patient information in medical notes.
- Schedule and complete study assessments, collect and prepare biological samples, and train other team members.
- Assist with trial set-up and coordination, and consult with Principal Investigators and Sponsors.
About Our Organisation
University College London Hospitals NHS Foundation Trust (UCLH) provides academically led acute and specialist services to a large and diverse population. We aim to deliver top-quality patient care, excellent education, and world-class research.
We have eight sites across London, providing first-class services in various specialties, including oncology, haematology, and neurology.
As a Clinical Trials Practitioner, you will be expected to develop specialized skills and knowledge relating to the conduct of clinical trials and work collaboratively with our multidisciplinary team to provide expert care to our patients.
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