- Dana-Farber Cancer Institute (Brookline, MA)
- …specimen tracking systems (STIP) and laboratory binders. + May be responsible for IRB and regulatory submissions and maintenance of regulatory files. ... Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. There is no responsibility to consent eligible… more
- Harvard University (Cambridge, MA)
- …lab; write and submit proposals to fund the research; secure and maintain IRB and regulatory approvals; conduct analysis, publish findings, and disseminate ... research findings through presentations; (2) act as scientific liaison for day-to-day oversight of research activities between Harvard Medical School and project sites in Texas, including conducting and leading data analyses across the study components;… more
- Children's Hospital Boston (Boston, MA)
- …appropriate conclusions, and effectively communicate results to team. Manage and direct regulatory / reporting activities related to projects (eg, IRB , updates/ ... appropriately informed. + Support research and project management for Divisional or Institutional projects across all phases of the project life-cycle. Develop tools… more
- Beth Israel Lahey Health (Boston, MA)
- …compliance with the study protocol; study site and project committee communication, regulatory documentation for the study, and overall study management. This role ... visits for subjects. (essential) 7. Assists investigator with correspondence with IRB . (essential) 8. As needed, may function in areas/clinics performing job… more
- Beth Israel Lahey Health (Boston, MA)
- …limited patient assessments such as collection of electrocardiograms. There may be regulatory and quality exposure in this position. The position typical hours will ... visits for subjects. (essential) 7. Assists investigator with correspondence with IRB . (essential) **Required Qualifications:** + Bachelor's degree required. + 0-1… more