Provides administrative support to the CRAs and project teams in accordance with ICH GCP, NovaTrials SOPs and local regulations. CTA Ensures clinical trial administration is performed such that the subjects’ rights, safety and wellbeing are protected and that the clinical trial data are reliable.
Job components:
- Serves as a member of the project team with the goal to contribute towards efficient management of clinical trials
- Manages inventories for clinical trials supplies
- Assists the project team with preparation and shipment of Clinical Trial documentation
- Develops and maintains the study specific investigator database
- Serves as an office based point of contact for all sites during the course of the study
- Sets up and maintains the Trial Master File (TMF)