Clinical Trials Coordinator - Research & Development
We are recruiting for a Clinical Trials Coordinator who shares our vision to be trusted to provide consistently outstanding care and exemplary service to our patients.
An exciting opportunity has arisen to join our Research team based at Mount Vernon Cancer Centre in Northwood, London for a 12 month period. The post involves working alongside Research Nurses and Clinicians to deliver research trials.
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 Research Nurses and wider Clinical Research Team.
You will be joining a well-established Research Team and a department which has over 100 members of research staff throughout the Trust.
At the heart of everything we do are our core values: Include, Respect, and Improve. We encourage you to embrace these values throughout the recruitment process and in your role with us.
Main duties of the job
1. Assist with the efficient and timely set up of clinical trials.
2. Maintain databases/spreadsheets and produce monthly progress reports on recruitment.
3. Assist with the tracking and raising of invoices, identifying discrepancies and escalating appropriately.
4. Manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines.
5. Assist with quality assurance of all trial related documentation in accordance with relevant legislation and guidelines.
6. Assist with preparation for audit and inspections within assigned teams.
7. General trial-related communication in accordance with the Data Protection Act.
Person Specification
Qualifications/Training
* Diploma or equivalent and/or relevant research experience.
* Relevant training courses in clinical research.
Previous Experience
* Experience in clinical trial administration including data management.
* Experience of working in a healthcare setting.
Knowledge
* Knowledge of the clinical trials process.
* Familiar with GCP guidelines/EU directives.
* Understanding of medical terminology.
* Knowledge of patient information systems.
Skills
* Good organisational skills.
* Good oral and written communication skills.
* Understanding of case report forms.
Other requirements
* Understanding of, and commitment to, equality, diversity and inclusion.
* Role model our Trust values every day.
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
£26,530 to £29,114 a year per annum plus 15% High Cost Area Supplement.
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