Clinical Research Coordinator - Multiple Myeloma

Coordinate and manage clinical trial data for the Multiple Myeloma program, providing primary data collection and management of patient clinical information for participation in clinical trials. Ensure timely trial assessments per protocol and collect protocol-related samples, including shipment to outside entities. Maintain participant trial binders and regulatory binders to ensure study compliance with state, federal, and IRB requirements; may handle IRB submissions. May screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants in the ONCORE system. Some travel may be required. Located in Boston and the surrounding communities. Collaborate with Protocol Scheduling, Materials Management, Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments. Prepare for internal and external audits and site monitoring visits. Manage clinical trials lifecycle from start-up to close-out, including communication with sponsors and regulatory authorities; contribute to research publications. Interact with study participants as required by protocol. Ensure accurate data entry of Visit Tracking and other trial-related information into the Clinical Trial Management System. Excellent organization, communication, and attention to detail are required; proficiency with Microsoft Office and discretion in handling confidential information.