Study Coordinator
Contract length: 2 month initial contract
Location: London
Rate: £18-£21 per hour PAYE
· ASAP start date
· DBS will be needed
· 1 stage interview process
An exciting opportunity has come to light, with that opportunity being the chance to work as a Clinical Study Coordinator for an NHS facility. The ideal candidate will be organised, have great communication skills, and have a strong interest in clinical research. The successful individual will play a crucial role within the research team ensuring the study is safe to conduct and the patient’s safety and wellbeing are of the highest priority.
Key responsibilities:
- Provide support to investigators on study feasibility, ethical approval procedures and research governance
- Looking after site files
- Managing the booking systems
- Contacting patients
- Working with external agencies
- General admin i.e., photocopy, emails
- Monitoring the activity across multiple studies
- Support the safe conduct of research to provide assurance that the rights, safety, and wellbeing of research participants are protected
- Manage all aspects of trial co-ordination as a key member of the clinical research team
Desirable:
- GCP
- Knowledge of medical research trials or university medical trials
- Excellent communication skills
- Excellent IT and literacy skills
- Organisational skills
- Ideally worked within the NHS previously
- Microsoft Office proficiency
If you would like more information on this role or think you would be a great fit, please do not hesitate to get in contact via email to Alannah.White@cpl.com
- Agency: Cpl Life Sciences
- Reference: JO-2305-516081
Website: Cpl Life Sciences
- Posted: 16th May 2023
- Expires: 13th June 2023
