Role Overview
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, contributing 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 includes transcribing accurate data from clinical notes into Case Report Forms (electronic or paper as required) in accordance with the clinical trials protocol and GCP. They will liaise with CRAs from the Pharmaceutical Industry and CROs, meet sponsor deadlines, and ensure efficient running of clinical trials.
They are also required to support a number of administrative duties related directly to the data capture and management of clinical trials.
Key Responsibilities:
* Transcribe accurate data from clinical notes into Case Report Forms
* Liaise with CRAs and sponsors
* Meet sponsor deadlines
* Ensure efficient running of clinical trials
* Support administrative duties related to data capture and management
Requirements:
* Excellent time management and problem-solving skills
* Attention to detail
* Ability to work as part of a multidisciplinary team
Benefits:
* EAP (Employee Assistance Programme)
* Staff Discounts
* Wellness Programs
* Pension Scheme
* Cycle to Work Scheme
* Health Services Staff Credit Union
* Annual Tax Saver Travel Scheme