The Multicenter CRA will perform the following duties under general supervision by the Clinical Research Manager:-Track the progress of the trial across all participating sites (e.g., accrual, biospecimen collection and transfer, reportable events, regulatory submissions)-Correspond with participating sites to support trial activities as needed-Answer questions about eligibility, study procedures or data entry-Prepare and distribute informational updates, including meeting minutes, missing data reports and safety reports-Communicate essential trial information and documentation, including protocol amendments; request routine updates from sites to maintain current study status-Facilitate database reviews and query resolution-Present the Sponsor-Investigator study status reports related to trial progress and assigned tasks-Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all inclusion/exclusion criteria-Conduct onsite and remote monitoring visits and complete corresponding monitoring reports (Domestic travel required for onsite monitoring)-Perform source document verification and drug accountability-Review study site regulatory binder and essential documents for completeness and accuracy-Evaluate ongoing protocol and data compliance-Issue, track and resolve queries-Gather, track and organize essential regulatory documents from participating sites-Facilitate and document Sponsor-Investigator review of safety reports, investigational drug brochure updates, study violations and adverse events-Submit routine and expedited reports to the FDA, IRB, funding sponsor or other stakeholders Qualifications . The Multicenter Program is an internal clinical trial operations team, specializing in the central coordination, monitoring and regulatory oversight of MGBCI investigator-initiated clinical trials that are expanded to participating sites outside of the Harvard Cancer Consortium.