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Clinical Trial Coordinator

Central London   •  Negotiable  •  Contract/Temporary, Full time

Clinical Trial Coordinator

Contract length: 4 months

Location: Central London

Start date: ASAP

Day rate: 150-170 PAYE

Interview process: 1 stage interview via Microsoft teams

A new opportunity to work for an academic institution within clinical research has come to light. In this Clinical Trial Coordinator position, you will assist in facilitating the set-up and running of several studies. You will be ensuring optimal data collection and participation in a monitoring program are run to ICH-GCP. You will also assist the Project Lead in developing and maintaining the CECM trials portfolio. The ideal candidate will be proactive, have effective written and verbal communication, and demonstrate a critical and intelligent attention to detail.


Maintaining and updating trial documentation, including trial specific procedures and case report forms (CRF).

Ensuring sites have all essential documents

Ensuring all current regulatory requirements are met and approvals are obtained.

Producing reports as required by the funder, Sponsor, ethics committee and regulatory authorities.

Ensuring biological samples are sent to central laboratories

Preparing protocol amendments for approval, as required, and disseminating them to sites.

Data collection and entry

Ensuring adherence to the protocol and responding to queries about the trial.

Ensuring prompt reporting of suspected unexpected serious adverse reactions and serious adverse events from sites and obtaining all relevant information.

Producing regular trial updates/newsletters etc. to sites.

Preparing and maintaining a trial risk assessment and monitoring plan

Liaising with site staff to resolve queries raised during monitoring visits.


Graduate in biological science or allied health field

Understanding of GCP

Knowledge of local and national clinical trial regulations

Previous experience in clinical trial research

Experience of existing UK clinical research structures, regulatory and ethical systems

Some experience of developing and maintaining clinical trial documentation (i.e. protocol, patient information sheets and case report forms)

Some experience of the Integrated Research Application System (IRAS) / CWOW

Demonstrable IT skills

If you would like more information on this role or think you would be a good fit, please contact Alannah.white@cpl.com or call 01189522797

  • Agency: Cpl Life Sciences
  • Contact: Alannah White
  • Reference: JO-2201-483655
  • Posted: 14th January 2022
  • Expires: 11th February 2022

Cpl Life Sciences

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