Clinical Trials Data Manager

START Dublin aims to provide patients with the opportunity to participate in early phase clinical trials. The post holder would be expected to work as part of a multidisciplinary team, to contribute to the delivery of START Dublin’s objectives in conducting clinical research, under the principles of Good Clinical Practice (GCP).

Purpose of the Role

The Clinical Data Manager will be responsible for all aspects of data management for all studies at START Dublin. This will include transcribing accurate data from clinical notes into Case Report Forms (electronic or paper as required) in accordance with the clinical trials protocol and GCP, liaising with CRA’s from the Pharmaceutical Industry and CRO’s, meeting sponsor deadlines and ensuring efficient running of clinical trials. They are also required to support a number of administrative duties which relate directly to the data capture and management of clinical trials.

Informal enquires can be made to: Niamh Ni Obain, Regulatory Affairs Specialist & Data Manager , START, niamhniobain@mater.ie