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Study Coordinator

Central London   •  Negotiable  •  Contract/Temporary, Full time


Study Coordinator

3-month contract

London

Rate: TBC

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 patients safety and wellbeing are of the highest priority.

Key responsibilities:

-Looking after site files

-Managing the booking systems

-Contacting patients

-Working with external agencies

-General admin i.e., photocopy, emails

-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
  • Contact: Alannah White
  • Reference: JO-2111-480843
  • Posted: 24th November 2021
  • Expires: 22nd December 2021

Cpl Life Sciences

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