Responsible for efficient processing and quality check of all study documents. Key Responsibilities:
* Support and organize the preparation of Clinical Study binders
* Supervision of clinical study applications/submissions to Ethical Committees and Competent Authorities as an administrative support function to the Study Managers;
* Support the Study Managers upon request from study managers based on project needs;
* Responsible for all document archiving;
* Control document validity and compliance (i.e. insurance certificates, etc.);
* Organization of meetings related to clinical investigations such as Clinical Event Committees, Data Safety Monitoring Boards, Executive Committees and Steering Committees
Sthree US is acting as an Employment Business in relation to this vacancy.