Country Approval Specialist - FSP - Italy
È questo il ruolo che sta cercando? Se sì, continui a leggere per maggiori dettagli e si ricordi di candidarsi oggi stesso.
As a Country Approval Specialist, you will help align country submissions with the global strategy while supporting site start-up processes. You will collaborate with internal and external teams to ensure timely site activation and adherence to regulatory standards. The role focuses on coordinating submissions, reviewing essential documents, and improving SSU metrics in a global, cross-functional environment. This is an opportunity to shape efficient start-up workflows at scale and contribute to clinical program success. You will work with diverse teams to drive timely, compliant country approvals and elevate overall study start-up performance.
Coordinate and manage country submissions in line with the global strategy
Support site start-up activities and document collection/review (ICF, FDF, 1572, CVs, etc.)
Collaborate with Study Startup, CROs,



Clinical Operations to improve SSU metrics
Ensure SSU standards are applied across projects
Identify and escalate potential site activation delays
Track actions and communications to meet study/site timelines
Resolve escalated issues with CROs/Clinical Operations in partnership with Study Startup
Provide feedback on site performance metrics and ensure eTMF accuracy during start-up
BS degree xysqume or international equivalent
2+ years of experience in clinical research Site Start Up
Ability to explain data to facilitate data-driven decisions
Knowledge of clinical study protocols and essential documents
Strong organizational, decision-making, communication, and negotiation skills
Proficient in Microsoft Excel, Word, and PowerPoint
Understanding of FDA and ICH-GCP guidelines
#J-18808-Ljbffr

📌 Country Approval Specialist - FSP - Italy (Cusano)
🏢 Experteer Italy
📍 Cusano