Clinical Trial Associate

Role: Clinical Trial Associate supporting early-phase hematologic disease studies at Disc Medicine. Responsibilities manage day-to-day clinical study activities, collaborate with Clinical Trial Managers, vendors, and CROs prepare and review study documentation ensure audit-readiness of trial files coordinate sample logistics and site start-up activities support study timelines, budgets, and trial updates and assist with regulatory document submissions. Requirements BA/BS, understanding of FDA and ICH GCP guidelines, proficiency in MS Office, excellent communication, initiative, and organizational skills experience in clinical project teams. Preferred experience in early-phase (Ph1) oncology or hematology trials familiarity with clinical data management and monitoring and ability to work in a fast-paced environment. HighValue: early-phase hematologic (blood disorders) clinical trials fully outsourced model cross-functional collaboration hybrid work setup in Watertown, MA no travel specified. #J-18808-Ljbffr