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Recruitment Coordinator

East London   •  £21 - 25 per hour  •  Contract/Temporary, Full time


Recruitment Coordinator

3-4 month contract

£18- £25 per hour

London

Have you ever wanted to play a crucial part in implementing a positive change to people’s lives? An NHS research study is currently looking for a Recruitment Coordinator with phlebotomy skills to join them and be a part of the positive change. The ideal candidate should possess the ability to work well as part of a team, but also be able to work independently. They should have excellent organisation and communication, compatible with educating subjects on their participation in clinical trials and have a solid working knowledge of Good Clinical Practice (GCP).

Key responsibilities:

· Work as part of a team of research active staff, coping with a flexible timetable to cover the clinical requirements of the CRF as efficiently as possible.

· Provide on-going advice and support to patients and families in the outpatient clinics and by telephone

· Develop and implement specialist care programmes (where appropriate) alongside the implementation of clinical trials and utilise professional background to deliver this.

· Assisting with pre-screening clinic assessments including obtaining blood samples and other appropriate pathological tests.

· Act as an on-going point of contact for patients, families and other health professionals relating to clinical trials.

· Working closely with the consultant and junior members of the clinical service and the research team to provide continuity of care.

· Work closely with the medical social workers.

· Develop links with other NIHR clinical research facilities throughout the UK to improve local systems identifying patients who may be eligible for clinical trials.

· Work with the Research and Development teams to collect metrics relating to clinical trial recruitment.

· Flexible finishing times as some of the afternoon clinics finish late.

Essential:

· Phlebotomy skills

· Possess a sound knowledge of the Clinical research process

· A solid working knowledge of Good Clinical Practice (GCP) and current legislation on clinical trials

· Basic computer literacy, MS word, Excel, and Email. Previous use of Electronic databases

· Previous experience in clinical research, medical or scientific environment

· Experience of working in a similar capacity within an ICH GCP research environment

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-2111-481145
  • Posted: 20th September 2022
  • Expires: 18th October 2022

Cpl Life Sciences

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