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