Overview
In questa posizione, you support study startup activities in Italy from our Milan site, ensuring timely and compliant activation of clinical sites. You’ll partner with cross-functional teams to manage regulatory, ethics, site documents, and contracts, while tracking startup timelines. The role blends operational execution with process improvements to accelerate site activation and study delivery. This opportunity suits a collaborative professional shaping clinical operations in a global pharma environment.

Retribuzione / Benefits
- base salary range provided
- premio
- incentive plans
- other benefits may apply

Responsabilità
- Support site identification and selection process
- Collect and review documents for ethics and regulatory review and approval
- Prepare site document packages for drug release to clinical sites
- Prepare and negotiate site contracts and budgets




- Communicate with project teams, investigational sites, review bodies, vendors, and clients regarding startup matters until site activation
- Monitor startup metrics and timelines
- Coordinate initiatives for startup process improvement, analyze best practices and challenges

Requisiti fondamentali
- College/University degree or equivalent
- At least 1 year industry experience in clinical research and/or 1 year of Study Startup experience in Italy
- Full working proficiency in English
- Strong communication and organizational skills
- Ability to negotiate and build relationships at all levels
- communication
- organizational skills
- negotiation
- relationship-building

📌 Study Startup Specialist I (Milano)
🏢 Psi Cro
📍 Milano