Clinical Research Coordinator
7 days ago
We are seeking a highly skilled and experienced Clinical Trials Coordinator to join our team at University College London Hospitals NHS Foundation Trust. As a Clinical Trials Coordinator, you will play a critical role in the coordination and management of clinical trials, ensuring the smooth delivery of high-quality research projects.
Key Responsibilities- Be the first point of contact for patients and their families, providing support and guidance throughout their clinical journey.
- Responsible for disseminating trial-related information to patients and obtaining their informed consent.
- Book all appointments and procedures, ensuring effective communication with patients and relevant clinical services.
- Ensure all administrative processes and procedures associated with clinical trials are followed according to protocol.
- Support the screening and recruitment of participants into the study, including attendance at Multidisciplinary Team (MDT) meetings.
- Work within the multidisciplinary study team, developing and maintaining 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 the senior research coordinator.
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, delivering top-quality patient care, excellent education, and world-class research.
Person Specification- Life Science or Nursing degree.
- Knowledge of clinical trials/observational studies.
- Knowledge of ICH GCP.
- Desirable: Knowledge of oncology and/or haematology.
- 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 prioritizing workload and meeting deadlines.
- Experience of independently carrying out a research project.
- Experience of working in a healthcare setting.
- Experience of dealing with patients and the public in a research setting.
- Experience of conducting clinical trials.
- Proven ability to prioritize own workload.
- Ability to acquire in-depth knowledge of study protocols and communicate this to professionals and lay people.
- Computer literacy, including experience of Word and Excel.
- Desirable: Phlebotomy skills.
- Proven ability to communicate effectively in writing.
- Good eye for detail.
- Ability to identify own training needs.
- Displays desire for professional and personal development.
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