Clinical Trials Coordinator
1 week ago
An exciting opportunity has arisen within the Research and Innovation Division at The Christie, for a Clinical Trial Coordinator within the GI Research Team
We are seeking an enthusiastic, motivated individual who will be responsible for assisting the research nurses, consultants and trial coordination management team with all aspects of clinical trial administration/ coordination.
Applicants should be qualified to at least diploma level, or have an equivalent level of experience.
The role is ideal for motivated individuals who are keen to gain experience in clinical trials administration and coordination.
As a Clinical Trials Coordinator you will be a valuable member of our team, with duties including; data management, case report form completion, invoicing, communication with trial sponsors, monitors and the wider research community, maintaining electronic records to support the team and assisting with the set-up of new studies.
The GI research team is a large clinical research team consisting of Research Portfolio Manager, Clinical Trial Coordinators, Clinical Research Nurses and a Research Nurse Team Leader who work closely with the medical team, recruiting and coordinating patients participating in clinical trials that will improve outcomes for patients with GI cancers. As a key member of the GI Research Team, you will be joining a busy, dynamic and supportive team with opportunities to learn and develop within the role.
The main purpose of the role is to support the clinical research team with all aspects of clinical trials administration, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies. The post holder will provide support to the Senior Clinical Trials Coordinators and wider Clinical Research Team.
The post holder will assist with the administration of clinical trials from feasibility to archiving including (but not limited to):
- Assist with the efficient and timely set up of clinical trials.
- Assist with the tracking and raising of invoices.
- Manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines.
- Assist with quality assurance of all trial related documentation in accordance with relevant legislation and guidelines.
- Assist with preparation for audit and inspections within assigned teams.
- General trial-related communication in accordance with the Data Protection Act.
- Assist with maintenance of clinical trial documentation.
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