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Study Coordinator

Central London   •  Negotiable  •  Contract/Temporary, Full time


Study Coordinator

2-3 month contract

London: 3 days on site, 2 days remote

20-25 per hour

CPL are urgently recruiting for an experience study coordinator to help support an NHS trust with the organisation of a number of on-going studies both outsourced and in-house studies. This is fantastic opportunity to grow your own skill set and contribute to leading research within the NHS.

Key responsibilities:

- Updating and managing site files

- Managing the booking systems including making appointments and scheduling

- Contacting patients for upcoming and follow up appointments

- General admin i.e., photocopy, emails and meeting minutes

- 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 are available to support the NHS on this contract then please apply here or send your CV to sarah.phillips@cpl.com.

A DBS check will be required for this role.

  • Agency: Cpl Life Sciences
  • Reference: JO-2205-492134
  • Posted: 9th May 2022
  • Expires: 6th June 2022

Cpl Life Sciences

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