FAQs
What is the duration of the Clinical Trials Coordinator position?
The position is for a 12-month period.
Where is the Clinical Trials Coordinator role based?
The role is based at Mount Vernon Cancer Centre in Northwood, London.
What are the main responsibilities of the Clinical Trials Coordinator?
The main responsibilities include supporting the clinical research team with trial administration, maintaining databases, producing progress reports on recruitment, and assisting with quality assurance of trial documentation.
What are the required qualifications for this role?
While specific qualifications are not listed, candidates should have experience in clinical trials administration and an understanding of Good Clinical Practice (GCP) guidelines.
Is there an opportunity for professional development in this role?
Yes, joining a well-established Research Team provides the opportunity for professional development and collaboration with experienced Research Nurses and Clinicians.
What values does the Trust prioritize in its employees?
The Trust values Include, Respect, and Improve, and it is important for candidates to embody these values during the recruitment process.
Is flexible working available for this position?
Yes, the Trust is committed to a positive work-life balance, and employees are entitled to seek flexible working patterns, which will be considered formally against service needs.
Who can I contact for further details or informal visits regarding the position?
You can contact Nadia Ahmed, the Clinical Trials Manager, at nadia.ahmed44@nhs.net or by phone at 0203 826 2403.