- General Dynamics Information Technology (Fairfax, VA)
- …Moderate expectations and Zero Trust-aligned security requirements. + **Translate DUAs, IRB and Privacy Board decisions, and data broker/licensing agreements** ... field (PhD, MD, or equivalent). + **Prior experience supporting Federal health, research or related agencies** on...and accident insurance are provided or available. We regularly review our Total Rewards package to ensure our offerings… more
- University of Utah (Salt Lake City, UT)
- …notifications and submits amended protocols, summaries and consents to the Institutional Review Board ( IRB ). 6. Submits study start-up applications, ... process improvements. 10. Maintains current knowledge of federal and institutional guidelines and requirements governing research . 11. Maintains regulatory… more
- 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