Take your career to the next level and be involved in study startup processes in India. You will provide operational support to project teams and ensure that PSI clinical projects start smoothly and on time.
Key Responsibilities:
- Develop site-specific startup timelines and meet the site activation targets
- Provide progress updates on the selected assigned projects and regular updates to all functions concerned
- Collect, review, and submit documents for ethics and regulatory review and approval (including review of 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
