ppAt bFortrea /b, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them. /ppWe’re now hiring a bStudy Start-Up Lead /b to join a sponsor‑dedicated team and drive the successful planning and activation of clinical trials. If you are passionate about accelerating study timelines, using data to guide decisions, and mentoring study start-up teams — this role offers you the opportunity to create a real impact. /ph3Why join Fortrea? /h3ulliWork in a collaborative, global environment with experts passionate about improving clinical research. /liliInfluence data-driven study start-up strategies for large-scale international programs. /liliPlay a key role in optimizing processes, bringing fresh ideas, and driving continuous improvement. /li /ulh3Your Main Responsibilities /h3ulliPartner closely with Clinical Operations to improve study start-up metrics and implement optimized processes. /liliProvide leadership, oversight, and mentoring to the FSP Site Start-Up team supporting integral clinical programs. /liliDevelop and refine data-driven forecasting models, planning scenarios, and benchmarking tools. /liliCreate country-specific Informed Consent Forms (ICFs) based on master templates and local requirements.



/liliEnsure SSU standards are applied consistently across projects and support ongoing process improvements. /liliLead data collection and analysis to influence SSU timelines and strategic decisions. /liliUse leading industry data sources and tools to support forecasting, site readiness insights, and cycle-time optimization. /liliAgree on site-level deliverables with internal teams; identify delays early and escalates when needed. /liliDrive delivery of “Ready to Enroll” status for both sponsor and CRO-supported sites. /liliServe as the escalation point for site activation challenges, partnering with Study Managers to resolve issues. /li /ulh3What You Bring /h3ulliBachelor’s degree in Life Sciences (or international equivalent). /lili4+ years of experience in clinical operations, project management, SSU, or trial optimization. /lili2+ years directly managing site activation and study start-up processes within a sponsor or CRO. /liliProven experience with country-level ICF creation. /liliStrong proficiency with data models, forecasting tools, and database structures. /liliExperience working in global site start-up environments strongly preferred. /liliAbility to explain complex data clearly and support data-driven decision-making. /liliExpert understanding of factors that drive successful study start-up and site selection strategies. /li /ulpLearn more about our EEO Accommodations request here. /p /p #J-18808-Ljbffr

📌 Sponsor Dedicated Site Startup Lead - Spain (Madrid)
🏢 Fortrea
📍 Madrid