- Mayo Clinic (Rochester, MN)
- …equity and inclusion, and provides the resources you need to succeed. **Responsibilities** The Institutional Review Board ( IRB ) Specialist is primarily ... responsible for the management of a caseload of applications submitted for IRB review and demonstrates sound judgment, as well as analytical, organizational, and… more
- Mayo Clinic (Rochester, MN)
- …provides the resources you need to succeed. **Responsibilities** Responsible for operation of the Institutional Review Board ( IRB ) activities in a manner ... goals; as well as, federal regulation and guidance. Supervises IRB staff conducting review and/or approval of...years of relevant Human Subject Research experience. Expertise of Institutional Review Board policy and… more
- Essentia Health (Duluth, MN)
- …for research proposals involving human subjects, including consent documents + Provide information to Institutional Review Board ( IRB ) members on ethical ... and apply federal and state laws and regulations and institutional policies that protect human subjects and research processes...issues and regulatory topics pertinent to IRB reviews + Oversee the quality assurance monitoring of… more
- Mayo Clinic (Rochester, MN)
- …with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board ( IRB ) document preparation and ... principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. + Collaborate with research team to assess feasibility and… more
- Mayo Clinic (Rochester, MN)
- …with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board ( IRB ) document preparation and ... principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. + Collaborate with research team to assess feasibility and… more
- ZOLL Medical Corporation (Minnetonka, MN)
- …clinical trial reports, regulatory reports and/or committee reports as needed. + Manage Central Institutional Review Board ( IRB ) for assigned trials. + ... the clinical investigational plan and the monitoring plan. + Review and approve monitoring reports. + Train Clinical Affairs...Thorough understanding of ICH GCP guidelines and ability to review and evaluate medical data. + Strong written, verbal,… more
- Fairview Health Services (Maplewood, MN)
- …consent process with potential research subjects in accordance with all regulatory, ethical and Institutional Review Board ( IRB ) requirements + Conducts ... + Collaborates with team members in preparing regulatory documents, including IRB application, informed consent, and recruiting materials + Educates internal and… more