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Clinical Trials Coordinator
2 months ago
We are seeking a highly skilled and experienced Clinical Trials Coordinator to join our team at University College London Hospitals NHS Foundation Trust. The successful candidate will play a crucial role in supporting the growth of our cancer clinical trials portfolio.
Key Responsibilities- Act as the primary point of contact for patients and their families, providing information and support throughout their clinical journey.
- Disseminate trial-related information to patients and obtain informed consent.
- Coordinate and manage the screening of patients, coordination of observational studies, and follow-up of Cross Tumour Trials Portfolio.
- Ensure all administrative processes and procedures associated with clinical trials are followed according to protocol.
- Ensure the safety and well-being of study participants is the primary concern.
- Support the screening and recruitment of participants into the study, including attendance to Multidisciplinary Team (MDT) meetings.
- Work collaboratively with the multidisciplinary study team to develop and maintain an understanding of disease processes relevant to the study.
- Maintain clinical skills relevant to the study, including phlebotomy, buccal swabs, and medical history.
- Collect and ensure the appropriate storage and transfer of biological samples as per the study protocol.
- Escalate any study/clinically related queries to the research nurse and/or senior researcher.
University College London Hospitals NHS Foundation Trust is one of the most complex NHS trusts in the UK, serving a large and diverse population. We provide academically led acute and specialist services, including cancer care, to people from the local area, from throughout the UK, and overseas.
We have a strong commitment to research and innovation, with a focus on improving patient outcomes and advancing medical knowledge. Our team is dedicated to delivering high-quality care and services, and we are seeking a talented and motivated individual to join our team.
Person SpecificationKnowledge and Qualifications:
- Life Science or Nursing degree.
- Knowledge of clinical trials/observational studies.
- Knowledge of ICH GCP.
Desirable:
- Knowledge of oncology and/or haematology.
Experience:
- Experience of working under minimal supervision.
- Experience of working as part of large teams and independently.
- Experience of working under own initiative.
- Experience of dealing with confidential information.
- Experience of planning and prioritising workload and meeting deadlines.
- Experience of independently carrying out a research project.
- Experience of working in a healthcare setting.
Desirable:
- Experience of dealing with patients and the public in a research setting.
- Experience of conducting clinical trials.
Skills and Abilities:
- Proven ability to prioritise own workload.
- Ability to acquire in-depth knowledge of study protocols and to communicate this to professionals and lay people.
- Computer literacy to include experience of Word and Excel.
Communication:
- Proven ability to communicate effectively in writing.
Personal and People Development:
- Good eye for detail.
- Ability to identify own training needs.
- Displays desire for professional and personal development.