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Study Coordinator

East London   •  Negotiable  •  Contract/Temporary, Full time

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



- 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
  • Posted: 16th May 2023
  • Expires: 13th June 2023

Cpl Life Sciences

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