Associate Clinical Trials Monitor - Preston, United Kingdom - University of Central Lancashire

Tom O´Connor

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Description

The University of Central Lancashire wishes to recruit an Associate Clinical Trials Monitor to join the Trial Management Team (under the leadership of Senior Clinical Trials Manager) to support the planning, co-ordination, and completion of clinical trial monitoring activities including the development of trial specific monitoring plans.

To be responsible for contributing to and supporting effective trial monitoring as part of the Trial Management Team ensuring good clinical practice within current legislative and governance frameworks.


Duties will include supporting the management of trial sites, provide support to sites on trial monitoring related matters including AE, SAE, IME incidence reporting, data queries, organisation of source files, monitoring procedures and schedules, reporting on such matters to the Trial Management Team/Senior Clinical Trials Manager.

Contribute to the work of Principal Clinical Trials Manager, Trials Management Team, Principal Investigators, and relevant stakeholders in their identification of resource implications of monitoring activities, travel and project timeline.

Implement and maintain trial site monitoring administrative systems ensuring that all key responsibilities are met.

Take responsibility for producing and maintaining trial monitoring plans and site-specific reports, ensuring that all documents and approvals are current.

Applicants need to meet all essential criteria on the person specification to be considered for interview. This position is based in Preston.


School/Service:
Lancashire Clinical Trials Unit


Contract Type:
Fixed term contract for 12 months

**Interview Date: To be confirmed

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