Regulatory Specialist – Study Start-Up

Location: Eastern Standard Time Hours Position Overview UniTriTeam is seeking a detail-oriented and proactive Regulatory Specialist – Study Start-Up to support our client in executing efficient, compliant study start-up activities across their clinical trial portfolio. This role is dedicated to accelerating study activation timelines while also supporting a critical migration from Complion to Florence eRegulatory. The role will include regulatory start-up execution, as well as data entry, document cleanup, and quality control activities to ensure a seamless transition to Florence. Key Responsibilities Study Start-Up & Regulatory Submissions Prepare, compile, and submit regulatory documents to IRBs/ECs…