Country Approval Specialist

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7dupjy

Country Approval Specialist - FSP - Italy

Se è interessato/a a candidarsi per questo lavoro, la preghiamo di assicurarsi di soddisfare i seguenti requisiti, elencati di seguito.
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.

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- 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 or international xysqume 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

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7dupjy