- Sanford Health (Sioux Falls, SD)
- … IRB is never boring but always rewarding. **Job Summary** The Institutional Review Board ( IRB ) Specialist ensures submitted research is reviewed ... detailed in Sanford Institutional Review Board Policy. Serves in role of IRB ...job (OTJ) training. OTJ training includes two years of Institutional Review Board ( IRB… more
- AdventHealth (Orlando, FL)
- … I, provides regulatory support to the research team by handling all of the Institutional Review Board ( IRB ) and regulatory submissions and maintenance ... Specialist I, functions as a liaison between the IRB of record for each study protocol and the...experience in healthcare, clinical research or scientific setting, an institutional review board office, or… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Research Staff Council monthly meetings + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... Research Staff Council monthly meetings + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional… more
- Houston Methodist (Houston, TX)
- …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... relationships with key study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure… more
- Magellan Health Services (Falls Church, VA)
- …subject matter expert to Institutional Officials, Human Research Protections Officers (HRPOs), Institutional Review Board ( IRB ) members and staff, ... will assist with oversight of human research protection programs, Institutional Review Boards (IRBs), human subject protection...a final Assessment report or summary. + Headquarters Level Review of IRB reviewed protocols for which… more
- Stony Brook University (Stony Brook, NY)
- …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. + Creating Institutional Review Board ( IRB ) submissions and ... Investigator Initiated Trial Specialist - Clinical Trials **Position Summary** The Cancer...managing correspondence across research sites, particularly in single- IRB /multi-site studies. + Planning and implementing changes to the… more
- Charles River Laboratories (Northridge, CA)
- …will also oversee the management of regulatory documentation related to the organization's Institutional Review Board ( IRB ) activities. Will assist ... records and spreadsheets related to the job functions. * Review batch records and release products. * Revise/ review...as deemed necessary. * Manage documentation associated with all IRB activities related to sponsor and study site submissions… more
- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- University of Pennsylvania (Philadelphia, PA)
- …B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB , ... assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB , including… more
- Johns Hopkins University (Fort Defiance, AZ)
- …and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific documentation ... a **_Sr. Compliance Monitoring Specialist_** . There are several Institutional Review Boards (IRBs) that we report...the FDA or commercial sponsors. + Assist in the review of IRB action outcomes, including the… more