Clinical Trials Officer
About the Role
Provide support to Principal Investigator and senior research nurse to set up appropriate research management systems to
comply with ICH-GCP, ISO 14155, local, national and international policies and legislation Co-ordinate and manage the
exchange of information between the study co-ordinating centre, clinical departments and Research & Innovation
department. Complete appropriate databases to record patients recruited to trials, track their visits and submit
information to finance department who invoice for commercial studies Review protocols for trials in order to prepare
appropriate labels, clinic sheets and study forms on Trust headed paper, for use during the trial. Ensure the accuracy
Responsibilities
- Perform core duties as described.
Requirements
- Relevant experience or willingness to learn.
Benefits
- Benefits per job description.
Compensation
To be discussed.
Location & Schedule
Per job description.
How to Apply
Use the “Apply” button.