- CUNY (New York, NY)
- …and exempt review decisions. + Manages and develops IRB review processes, including protocol distribution for full board and expedited reviews, and ... Oversees regulatory compliance across multiple domains, including the Human Subjects Research Program (HSRP), Export Controls, IRB agreements, approvals,… more
- Johns Hopkins University (Baltimore, MD)
- …serious adverse event reporting with the investigators to ensure prompt reporting to the IRB , DSMB, and study sponsor + Review protocol amendments to identify ... trials. + Experience with budgeting, invoicing, NIH and/or Department of Defense research progress reports, IRB management. + Petty cash disbursement and… more
- Mount Sinai Health System (New York, NY)
- …and training to multiple study teams who develop and submit documentation and information for Institutional Review Board ( IRB ) review and who ... revises regulatory standard operating policies and procedures. + Submits protocol applications for IRB review in a timely manner; tracks new protocols through… more
- University of Washington (Seattle, WA)
- …department in compliance with UW, federal , and state policies and regulations. + Review proposals for potential IRB , IACUC and SFI issues and work with PIs ... + Provide regular updates to faculty and department administrators regarding changes in federal and university research directives, as well as changes to… more
- Georgetown Univerisity (Washington, DC)
- …managers, and clinical trial sponsors. The role also requires frequent communication with the Institutional Review Board ( IRB ) and compliance offices. ... clinical research studies + Ensure compliance with institutional , federal , and sponsor regulations + Communicate...with regulatory and ethical requirements related to human subjects research (eg, IRB , + Strong attention to… more
- Stony Brook University (Stony Brook, NY)
- …GCP guidelines, and institutional policies. Responds to all questions from the IRB related to the regulatory aspects of the study. + Creates and maintains files ... systems and Clinical Trial Management Systems. Direct experience with IRB submissions to BRANY and Stony Brook IRB...subjects. + Create research records (eg a research binder) for each participant by chart review… more
- Rush University Medical Center (Chicago, IL)
- …(CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) strongly ... continuing review applications and unanticipated problems. * Communicates with IRB and finalizes documents based on IRB comments and recommendations… more
- Cedars-Sinai (Los Angeles, CA)
- … organizations, where applicable. **Primary Duties and Responsibilities:** + Submits research projects (protocols, consent forms, recruitment materials, IRB ... report forms, SAE's and source documents to ensure that research is being conducted according to IRB ,...IRB . + May help coordinate and prepare for institutional , pharmaceutical and internal audits. + Coordinates site feasibility… more
- University of Pennsylvania (Philadelphia, PA)
- …private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Department of Cardiovascular Surgery) Job Profile...AEs and SAEs are reported to the sponsor and IRB per protocol. The CRC will participate in clinic… more
- Dana-Farber Cancer Institute (Boston, MA)
- …entities as required. Maintains regulatory binders and ensures study compliance with all state, federal , and IRB requirements. May be responsible for IRB ... The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking...start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site… more