In this role you lead the initiation of clinical trials, ensuring regulatory compliance and supporting the advancement of new treatments. You collaborate across the Study Startup team, CROs, and Clinical Operations to optimize site activation timelines and maintain accurate documentation. You will monitor site performance, address activation delays, and ensure eTMF quality. This position offers the chance to impact trial timelines and improve SSU processes in a values-driven environment.
Health and wellbeing programmes
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes
Learning and development opportunities
Coordinate site start-up and activation activities and deliverables
Collaborate with internal Study Startup team, CROs, Clinical Operations, and TAU partners to improve SSU metrics
Ensure adherence to SSU standards across projects
Identify and elevate potential site activation delays
Track actions and communications to meet study/site timelines
Resolve escalated issues in partnership with CROs and Clinical Operations
Provide feedback on site performance metrics to management
Ensure accuracy and completeness of the eTMF for assigned sites during start-up
BS degree or international equivalent
2+ years of experience in clinical research Site Start Up within pharma, CRO, or relevant vendor
Ability to translate data into informed decisions
Knowledge of clinical study protocols and essential documents
Strong organizational, decision-making, communication, and negotiation skills
Proficiency in Microsoft Excel, Word, and PowerPoint
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📌 Study Start Up Associate Ii (Milano)
🏢 Altro
📍 Milano