To support Breast Oncology clinical research projects, the full-time Regulatory Coordinator - Massachusetts will manage protocol submissions, prepare regulatory documents, and maintain compliance records while working remotely with occasional on-campus meetings in Boston. Key responsibilities Prepares and submits protocol applications, amendments, and informed consent documents for review and approval Maintains and organizes regulatory files for assigned studies in compliance with sponsor requirements Tracks and manages new protocol start-up packets, ensuring established benchmarks are met Required qualifications Bachelor's degree or 1 year of experience as a Dana-Farber Associate Regulatory Coordinator 0-1 years of experience in a medical, scientific research, or technology-oriented environment preferred Basic understanding of clinical trial conduct Proficiency in Microsoft applications and databases Experience with medical terminology