Regulatory Coordinator - Massachusetts

Working remotely with occasional on-campus presence in Boston, the full-time Regulatory Coordinator - Massachusetts will manage regulatory submissions, maintain compliance records, and collaborate with clinical trial stakeholders to support Breast Oncology research projects. Key responsibilities Prepares and submits protocol applications, amendments, and informed consent documents for review and approval Maintains regulatory files and tracking databases to ensure compliance with study sponsor requirements and regulatory agencies Facilitates communication among study team members, sponsors, and regulatory agencies regarding study status and compliance 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 business environment preferred Basic understanding of clinical trial conduct Proficiency in Microsoft applications and databases Experience with medical terminology