Clinical Research Coordinator - Brighton

Coordinate clinical trials at the Dana-Farber Brighton Satellite site as part of the clinical research program, handling primary data collection, management of patient information, regulatory documents, and IRB submissions under GCP. Responsible for regulatory binders, regulatory tracking, source document collection, adverse event reporting, and data queries; assist with protocol eligibility screening, informed consent (minimal risk studies), and participant registration. May involve organizing regulatory reports, site activations, and travel between satellite locations to support study activities. Strong emphasis on data management, regulatory compliance, coordination with study teams, sponsors, and regulatory authorities; requires organization, attention to detail, and effective communication. Minimum qualifications include a bachelor’s degree and 0–1 year of related experience with preferred background in medical or scientific research; role involves minimal patient contact and travel between sites as needed.