As a Study Startup Associate at PSI CRO AG, you will be involved in the study startup processes in India, providing operational support to project teams to ensure clinical projects start smoothly and on time.
Key Responsibilities:
- Develop site-specific startup timelines and meet site activation targets
- Provide progress updates on assigned projects and regular updates to all concerned functions
- Collect, review, and submit documents for ethics and regulatory review and approval, including study-specific translations
- Facilitate site budgets and contract negotiations
- Prepare packages of site documents for drug release to clinical sites
- Maintain study-specific and corporate startup tracking and filing systems
