Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, eco-friendly campus with an on-site fitness center RTD Eco Pass Secure bike storage room Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility. • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); • Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards); • Maintain timelines for study start-up through both internal and external collaboration; • Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; • and Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges.