Site Selection Lead I

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

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

• Oversee the successful delivery of global site identification and selection in collaboration with the Feasibility Director/Lead. • Enable study teams to conduct effective and ongoing delivery within timelines that contribute to operational planning. • Assist in the evaluation of sites and investigators based on a data-driven study strategy. • Collaborate with Feasibility Lead/Director and Study Start-up team members in relation to the site identification and selection strategy. • Support Feasibility Lead/Director in final selection of sites.

🎯 Requirements

• BS degree or international equivalent required, in a life science preferred. • At least 2 years of pharmaceutical industry (or similar) experience. • Direct responsibility in site identification, feasibility, and/or managing the study start-up processes of clinical research studies at a sponsor or CRO is preferred. • Expertise with leading edge trial optimization vendors, tools, and methods. • Proficiency with software models, database structures, and Microsoft Office Suite applications. • Expertise in principles driving country/site identification desired. • Direct experience in the pharmaceutical industry or related field required. • Ability to strongly demonstrate, interpret, explain, represent, present and drive unbiased data insights into clinical trials operational planning. • Ability to work across several projects with specific and unique requirements, while providing attention to detail and high-quality work. • Ability to be flexible, adapt to change, work independently, as well as work as part of a team in a matrix environment.

🏖️ Benefits

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers) • 401(K) • Paid time off (PTO) • Employee recognition awards • Multiple ERG’s (employee resource groups)