Clinical Trial Coordinator

Clinical Trial Coordinator

Contract length: 4-5 months

Location: Central London

Rate: £35k - £37k per annum, pro rata (hosted)

Start date: ASAP

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.

Responsibilities:

•      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.

Requirements:

·       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 [email protected]