Take your career to the next level and be involved in study startup processes in Italy. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time.
This role is hybrid in our Milan office
You will:
- Support site identification and selection process
- Collect and review documents for ethics and regulatory review and approval
- Prepare packages of site documents for drug release to clinical sites
- Prepare and negotiate site contracts and budgets
- Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding startup matters till the moment of site activation
- Monitor startup metrics and timelines
- Coordinate initiatives for startup process improvement, analyze best practices and challenges