Clinical Research Coordinator

2 months ago

London, Greater London, United Kingdom University College London Hospitals NHS Foundation Trust Full time
About the Role

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.
About Us

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.
Essential 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 prioritizing workload and meeting deadlines.
  • Experience of independently carrying out a research project.
  • Experience of working in a healthcare setting.
Desirable Experience
  • Experience of dealing with patients and the public in a research setting.
  • Experience of conducting clinical trials.
Skills and Abilities
  • 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.
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.

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