Trial Administrator

Your Responsibilities

What you’ll do

  This post represents an excellent opportunity within clinical research.

You will be working on site to help provide support to embedded research teams across the trust for new and existing studies.

You will be involved in supporting all administrative aspects of the research process, including liaising with and arranging appointment times for patients, data entry and management for a variety of databases, compiling study folders, preparing documents for monitoring, meeting planning and general administrative duties.

What we’re looking for

We are looking for a highly motivated, Clinical Trials Administrator to work as part of our Quality Assurance Team working between the Southampton General and Royal South Hants Hospital sites, to assist in the development, implementation and maintenance of systems to assure the quality of clinical research undertaken within the CRF, in accordance with a variety of regulatory Statutes, guidelines and protocols as required by the by the Medicines and Healthcare Products Regulatory Agency (MHRA), the Health & Safety Executive, the Human Tissue Authority and other regulatory agencies.

Assist the CRF Quality Assurance team as required for Governance and Quality Assurance (QA) initiatives linked to the research programmes to ensure that the WTCRF and BRUs meet standards for the conduct of clinical trials.  This work is to be carried out locally in collaboration with R&D RG&QA Manager, CRF Matron and Operations Managers and nationally within the QA group of the Clinical Research Facilities UK Network.

This is an exciting and excellent opportunity to join a vibrant team with extensive expertise in clinical research.

This post forms part of a team created to drive and deliver an exciting Research agenda and achieve our vision of being one of the best. We are dedicated to providing high quality, patient-centred research within a state-of-the-art clinical research facility.