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Clinical Trial Coordinator

Clinical Research

Compass Life Sciences are privileged to be partnering exclusively with an emerging CRO supporting in their search to appoint a Clinical Trial Coordinator at a new state of the art facility.

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Compass Life Sciences are privileged to be partnering exclusively with an emerging CRO supporting in their search to appoint a Clinical Trial Coordinator at a new state of the art facility.

The Clinical Trial Coordinator will be responsible for the set up and delivery of clinical trials in accordance with GCP Guidelines and in line with operational, financial, and developmental strategies with the organisation. Other key responsibilities include, assisting in preparation for sponsor CRO and regulatory audits and inspection. As well as managing the clinical trial operations including participants and any external vendors, responsibilities of this role will also include, but are not limited to;

  • Accountability for ICH-GCP compliance across all assigned studies
  • Support the development of the business by working closely with clinicians and consultants to maximise business opportunities and recruit patients
  • Adhere to the organisation's policies and SOPs and ensure all members of the clinical trials team are trained and compliant
  • To ensure that all administration is performed accurately and in a timely way including the entry of patient records on all necessary databases and forms
  • Maintain all patient records so that they are accurate, stored appropriately and all confidential information is retained in accordance with GDPR
  • Ensure adequate stock within the Centre ensuring that it is ordered in a timely way and that stock is controlled
  • Complete the necessary start-up activities including assisting the Clinical Trials Start Up Specialist with any completion and submission of Non-NHS SSI forms to the relevant REC for new studies to be conducted at the Centre as and when required
  • Perform internal audits of working practices within the Centre to measure compliance against company SOPs and GCP as and when required


To be considered for this opportunity, the ideal candidate will have:

  • Degree in a relevant scientific background
  • Previous experience in clinical trial research
  • Proficiency in the use of Microsoft Office packages (Word, Excel, PowerPoint)
  • A background working with Electronic Data Capture systems (EDC)

Given the nature of the trials involved, previous experience in Cognitive studies would be advantageous but not essential, and the ideal candidate will preferably come from a background as a Clinical Trial Coordinator in a private health sector.
In exchange for this our client is offering

  • Competitive salary
  • Professional development opportunities
  • Private Health Insurance
  • Life insurance
  • Pension scheme
  • Various other soft benefits

If you would like to be considered for this opportunity please get in touch with Ben Brown on 02393874320 or [email protected]


Not for you but, know someone who might be interested?

Compass Associates Ltd. trading as Compass Life Sciences are acting as a Recruitment Consultancy for this permanent vacancy; we offer up to £1,000 worth of John Lewis or Amazon Vouchers or alternatively, an equal donation to a charity of your choosing for each successful recommendation.

Apply for the position of Clinical Trial Coordinator now with Compass Life Sciences

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* If my CV contains any special category data e.g. race; ethnic origin; political views; religious beliefs; trade union membership; health information; or sexual orientation, I consent to this data being processed by Compass Life Sciences as part of my job application.