Apprentice Clinical Trials Coordinator
3 days ago
This is a 24-month contract inclusive of an 18 month apprenticeship.
**Band 4 Annex 21 for the duration of the apprenticeship**: First 6 months - £18,397pa; Next 12 months - £19,711pa. On successful completion of the apprenticeship the salary will be £23,949pa for the remainder of the contract
You will be based within the GI research delivery team at The Christie, supporting a large number of commercial, NCRN and clinician-led trials.
As an Apprentice Clinical Trials Coordinator you will be trained to be a valuable member of our team, providing support such as assisting the research nurses, consultants and trial administration/ coordination management team with various aspects of clinical trial administration/ coordination work 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 Christie NHS Foundation Trust is one of the leading cancer centres in Europe, offering high quality diagnosis, treatment and care as well as being at the forefront of cancer research and education.
As a key member of the GI research delivery team, you will be joining a busy, dynamic and supportive team.
The role is ideal for individuals keen to gain experience in clinical trials coordination.
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 be supported to undertake the Level 3 Business Administrator apprenticeship qualification alongside the AMSPAR Level 2 Award in Medical Terminology qualification.
Duties are separated into those the postholder can do from Day 1 (in standard font) and those they will progress into over time.
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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