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Clinical trials coordinator
Alfianni Online - Artist Netwerk
Newcastle upon Tyne
On-site
GBP 60,000 - 80,000
Full time
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Job summary
An established industry player is seeking a Clinical Trials Coordinator to join their multi-disciplinary team. This entry-level position is crucial for the setup and delivery of a diverse portfolio of clinical trials, ensuring compliance with national and local policies. The role emphasizes adherence to Good Clinical Practice and the EU directive for clinical trials. The organization values flexibility, offering a supportive environment where you can discuss your working arrangements. If you are passionate about advancing clinical research and want to make a difference in patient care, this role is perfect for you.
Qualifications
- Understanding of clinical trial protocols and compliance requirements.
- Ability to manage multiple trials simultaneously.
Responsibilities
- Ensure clinical trials are set up and delivered according to national metrics.
- Report treatment events to relevant external trials organizations.
Skills
Education
Job description
The Clinical Trials Coordinator is an important role within the multi-disciplinary team responsible for the set-up and delivery of a high portfolio of clinical trials in line with national and local policies and guidelines. You will be responsible for ensuring that studies are set-up within national metrics and delivered in line with local expectations. The role will ensure trials are carried out and conducted in accordance with Good Clinical Practice, Research Governance Framework and are compliant with the EU Directive of Clinical Trials. To ensure any trials within the post holder's remit, carried out in the Clinical Trials Unit are properly conducted according to Good Clinical Practice (GCP), Research Governance Framework and are compliant with the EU directive for clinical trials.
(There can be multiple trials at any given time, in various stages of preparation, inception and completion.) All events pertaining to the treatment of said patients are reported in the agreed timeframes to relevant external trials organisations. As a flexible working friendly organisation, we want to be sure that you can work in a way that is best for us and for our patients, and for you. Speak to us about how we might be able to accommodate a flexible working arrangement. If it works for the service, we will do our best to make it work for you.
- Entry level
- Full-time
- Science
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