To support Head & Neck Oncology clinical research, the full-time Regulatory Coordinator - Oncology will manage protocol submissions, prepare regulatory documents, and ensure compliance with applicable regulations while working remotely with occasional on-campus requirements in Boston, MA. Key responsibilities Prepares and submits protocol applications, amendments, and informed consent documents for review and approval Maintains and organizes regulatory files for assigned studies, ensuring compliance with sponsor requirements Communicates and collaborates with clinical trial stakeholders to track and manage study start-up progress and regulatory submissions 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 Familiarity with medical terminology