Job Description

We are assisting this global CRO in their search for a Clinical Systems Specialist. This role can be based from any of their European office.
The job holder will set up and maintain projects within the designated clinical systems used by project staff across Product Development, Europe. Additionally, the job holder will provide support for the designated clinical systems to a specific therapeutic project unit, a designated region (multiple offices), or local office.

Key responsibilities include:

Supporting projects within a specific therapeutic project unit in Product Development, Europe
setting-up and maintaining a project within the designated clinical system.
Ensuring the consistent use of designated clinical systems and/or procedures across projects within the assigned therapeutic project unit.
Conducting QC checks within a project, providing appropriate reports to PMs/CTLs to ensure better quality data
Providing support to a designated region (multiple offices) or local office for designated clinical systems.
Providing training on designated clinical systems to local and regional user(s) or project team(s). May be required to participate in customer demonstrations/presentations upon request.
Participation in user testing of new enhancements/functionality and/or review of associated procedures/training/documentation.
Maintaining awareness of overall developments in the field of clinical research.
Identifying and recording quality problems. Suggesting, initiating, recommending or providing solutions, as appropriate.
Knowledge of all relevant associated SOPS/Work Instructions.
Knowledge of financial and performance metrics to accomplish effectively assigned tasks and responsibilities.
To apply you will have a minimum of 2 years experience of working in a clinical research related environment. This will be further supported by:

An advanced working knowledge of designated clinical system(s) and/or process, applicable SOPs and regulations and understanding of system interactions/interdependencies.
An ability to independently conduct designated clinical system and/or process training, as well as customer demonstrations/presentations (as needed)
A knowledge and ability to work cross-functionally

Qualifications/Skills Required

2yrs experience of working in a clinical research related environment is preferable. An advanced working knowledge of designated clinical system(s) and/or process, applicable SOPs and regulations and understanding of system interactions/interdependencies.
An ability to independently conduct designated clinical system and/or process training, as well as customer demonstrations/presentations