FAQs
What is the primary role of a Clinical Trials Assistant in the General Surgery research team?
The primary role involves supporting a portfolio of clinical trials from study setup to archiving, ensuring compliance with clinical trial protocols and regulatory standards.
What tasks will the Clinical Trials Assistant be responsible for?
The Clinical Trials Assistant will be responsible for submitting documents for approvals, maintaining research data records, providing support to Research Nurses, processing samples, and assisting with recruitment processes.
What qualifications or experience are required for this role?
While specific qualifications or experience are not mentioned in the job description, a background in healthcare, research, or clinical trials would be beneficial.
Who should I contact for more information about this position?
You can contact Rebecca Pyecroft-Oxley, Trust Research Matron at r.pyecroft-oxley@nhs.net or Debby Hawkins, Directorate Research Coordinator at debby.hawkins@nhs.net for further details or informal visits.
What kind of studies will the Clinical Trials Assistant be involved with?
The Clinical Trials Assistant will support a wide range of studies, including those from the NIHR Sheffield Biomedical Research Centre (BRC) and the NIHR Sheffield Clinical Research Facility (CRF).
Is there potential for professional development in this role?
Yes, the Trust is committed to professional development and offers many policies to support employees in balancing personal and professional lives.
Will the Clinical Trials Assistant have the opportunity to manage their own studies?
Yes, post holders may support and be responsible for relevant studies in their own right in addition to their collaborative responsibilities.
How does the Trust value its staff?
The Trust values and respects all its staff and the community it serves, providing excellent benefits and support mechanisms.