- Saint Louis University (St. Louis, MO)
- …a liaison between the SLU SOM, clinical partners (eg, SSM Health), the Principal Investigator, Institutional Review Board ( IRB ), and sponsors to ensure ... in a variety of studies; develops and submits documentation and information for Institutional Review Board ( IRB ) review ; communicates with the… more
- Saint Louis University (St. Louis, MO)
- …a liaison between the SLU SOM, clinical partners (ex. SSM Health), the Principal Investigator, Institutional Review Board ( IRB ), and sponsors to ensure ... (GCP) throughout the life cycle of the study. PRIMARY JOB RESPONSIBILITIES Review and abstract medical record information and ensure proper adherence to… more
- Planned Parenthood (Minneapolis, MN)
- …supervision of the Research Manager. This position will focus on research study start-up, Institutional Review Board ( IRB ) submissions, study project ... Day-to-Day Responsibilities: Study Coordination and Reporting Independently develop and prepare Institutional Review Board applications, including completion… more
- University of Iowa Hospitals & Clinics (Iowa City, IA)
- …of the appropriate Human Subjects Review forms and application materials to the Institutional Review Board ( IRB -01) as well as external IRBs ... of multiple complex clinical studies. Serve as a liaison with IRB staff, regulatory authorities, and investigators and study coordinators. Coordinate external… more
- Cedars Sinai (Beverly Hills, CA)
- …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). What are the Primary Duties ... study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious… more
- Henry Ford Health System (Detroit, MI)
- …objectives of the established research protocol are met and in compliance with the Institutional Review Board ( IRB ) and sponsor guidelines. Identifies ... minimum of 5 years of RN research experience. Experience managing the project IRB is a plus Clinical knowledge and analytical abilities necessary to formulate… more
- Virginia Commonwealth University (Richmond, VA)
- …student research activities including funding and presentation opportunities. Assist students with Institutional Review Board ( IRB ) processes, including ... or student research symposia. Familiarity with research compliance and institutional processes related to IRB review...research compliance and institutional processes related to IRB review , responsible conduct of research, and… more
- BayCare Health System (Tampa, FL)
- …with the standards of good clinical practice, federal and state regulations and institutional review board ( IRB ) requirements Ensures adherence ... for protocol related procedures Screening, study recruitment, preparation of IRB reports Establishment and maintenance of regulatory documents Performing the… more
- Northwestern University (Chicago, IL)
- …local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration ... this clinical trial, including but not limited to (a) regulatory [e.g., IRB ] requirements, (b) ensuring study protocols for intervention delivery and data collection… more
- Kaiser Permanente (Oakland, CA)
- …guidelines, including those related to human subjects' research, research privacy, data management, Institutional Review Board ( IRB ) practices, and ... export controls. The manager will oversee compliance with regulatory requirements and liaise with regulatory agencies and bodies such as the Office for Human Research Protections (OHRP), Office of Research Integrity (ORI), and Food and Drug Administration… more
- Nuvance Health (Norwalk, CT)
- …patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... submits all study protocols, consent forms, and other required documents to the Institutional Review Board ( IRB ). 7. Educates hospital staff about… more
- Stony Brook Medicine (Stony Brook, NY)
- …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. Creating Institutional Review Board ( IRB ) submissions and ... managing correspondence across research sites, particularly in single- IRB /multi-site studies. Planning and implementing changes to the research...or for a maximum of 90 days. An initial review of all applicants will occur two weeks from… more
- Children's National Hospital (Washington, DC)
- …the development of action plans to improve quality. Facilitates the preparation of Institutional Review Board applications for research proposals, develops ... manage research and/or research intervention projects within the federal and institutional regulations and policies under the direction of the principal… more
- Northwestern University (Chicago, IL)
- …local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration ... related; OR appropriate combination of education and experience. Must complete NU's IRB CITI training before interacting with any participants & must re-certify… more
- The University of Pennsylvania (Philadelphia, PA)
- …Other duties and responsibilities as assigned Regulatory Responsibilities: Prepare and process all Institutional Review Board ( IRB ) documentation through ... Initiation meetings Obtain slides from pathology and ship to sponsor/independent review per protocol guidelines. Obtain records required to complete case report… more
- University of Massachusetts Medical School (Worcester, MA)
- …research related supplies Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board ( IRB ) processes Provide ... FUNCTIONS: Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA Identify, schedule… more
- The University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... team members in retrieval and provision of documentation required for IRB submission/renewals in accordance with guidelines; continuing review , modification,… more
- Kaiser Permanente (Oakland, CA)
- …guidelines, including those related to human subjects' research, research privacy, data management, Institutional Review Board ( IRB ) practices, and ... (ORI), and Food and Drug Administration (FDA). Demonstrated experience with Institutional Review Board ( IRB ) practices. Primary Location:… more
- Mount Sinai Hospital (New York, NY)
- …grant applications and documents and assists in protocol submissions (for eg, Institutional Review Board , Grants and Contracts Office). Responsibilities ... evaluation of the study subjects. 3. Prepares and ensures grant applications, IRB /GCO documents are submitted. 4. Ensures accurate and complete compilation of… more
- UC Davis Health (Sacramento, CA)
- …agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board ( IRB ), Food and Drug ... information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting… more
