12 ago - Milano
Fortrea
Why join Fortrea?Work in a collaborative, global environment with experts passionate about improving clinical research. Influence data-driven study start-up strategies for large-scale international programs. Play a key role in optimizing processes, bringing fresh ideas, and driving continuous improvement.
Legga la panoramica di questa occasione per capire quali competenze sono richieste, incluse le soft skill pertinenti e la padronanza di pacchetti software.
Your Main ResponsibilitiesIn this role, you will lead, guide, and empower site activation teams across multiple countries.
- Partner closely with Clinical Operations to improve study start-up metrics and implement optimized processes.
- Provide leadership, oversight, and mentoring to the FSP Site Start-Up team supporting global clinical programs.
- Develop and refine data-driven forecasting models, planning scenarios, and benchmarking tools.
- Create country-specific Informed Consent Forms (ICFs) based on master templates and local requirements.
- Ensure SSU standards are applied consistently across projects and support ongoing process improvements.
- Lead data collection and analysis to influence SSU timelines and strategic decisions.
- Use leading industry data sources and tools to support forecasting, site readiness insights, and cycle-time optimization.
- Agree on site-level deliverables with internal teams; identify delays early and elevate when needed.
- Drive delivery of “Ready to Enroll” status for both sponsor and CRO-supported sites.
- Serve as the escalation point for site activation challenges, partnering with Study Managers to resolve issues.
What You Bring
- Bachelor’s degree in Life Sciences (or international equivalent).
- 4+ years of experience in clinical operations, project management, SSU, or trial optimization.
- 2+ years directly managing site activation and study start-up processes within a sponsor or CRO.
- Proven experience with country-level ICF creation.
- Strong proficiency with d
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