Sponsor Dedicated Site Startup Lead

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• 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. • 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. • Drive delivery of “Ready to Enroll” status for both sponsor and CRO-supported sites. • Serve as the escalation point for site activation challenges.

🎯 Requirements

• 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 data models, forecasting tools, and database structures. • Experience working in global site start-up environments strongly preferred. • Ability to explain complex data clearly and support data-driven decision-making. • Expert understanding of factors that drive successful study start-up and site selection strategies. • Fluency in local language and English.

🏖️ Benefits

• Collaborative global environment with experts passionate about improving clinical research. • Opportunity to influence data-driven study start-up strategies for large-scale international programs. • Key role in optimizing processes and driving continuous improvement.