- UTMB Health (Galveston, TX)
- …Coordinates regulatory committee reviews of human subjects/animal protocols, including management of Institutional Review Board ( IRB ) committee/ ... HRPP/ IRB Office (Research, Regulatory, & Compliance - Galveston)...of protocol review management to assist the Institutional Review Board / Institutional … more
- Vitalief (Livingston, NJ)
- …will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure ... human subjects research. This role supports investigators, staff, and IRB members in the preparation, review , and...members. + Maintain compliance with OHRP, FDA, ICH/GCP, and institutional regulations. + Manage IRB databases, tracking… more
- Brown University (Providence, RI)
- …of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board ( IRB ) of record for Brown, Lifespan ... administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB ) policies and procedures related to… more
- University of Colorado (Aurora, CO)
- …**Description** **University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board - Office of Regulatory ... a year for year basis. **Preferred Qualifications:** + Experience working with Institutional Review Boards or OHRP/FDA regulations regarding human subject… more
- Johns Hopkins University (Baltimore, MD)
- …written reports of monitoring findings and recommendations for review by the Institutional Review Board . + Participate in Compliance Monitoring Program ... We are seeking an ** IRB Compliance Monitoring Specialist** who will be part...be part of a team that supports the JHM Institutional Review Boards (IRBs). This role conducts… more
- Cleveland Clinic (Cleveland, OH)
- …you will lead the Cleveland Clinic Human Subjects Protection Program and oversee all Institutional Review Board ( IRB ) operations, including policies, ... the enterprise. This role is responsible for the development, review and approval of IRB policies and...overseeing staff and ensuring adherence to federal, state and institutional policies + Collaborative mindset to work with researchers… more
- Johns Hopkins University (Baltimore, MD)
- …who will be part of a team that processes human subjects research protocols overseen by the Institutional Review Board ( IRB ). The IRB Coordinator is ... Duties & Responsibilities** + Demonstrate knowledge-based understanding of the complete IRB review process. + Provide administrative support and advice… more
- BayCare Health System (Clearwater, FL)
- …**Facility:** BayCare Systems Office (Hybrid) **Responsibilities:** + Provide functional support to the Institutional Review Board ( IRB ). + Responsible ... of IRB applications, maintenance of IRB files, preparation of IRB approval letters, initial application support, and pre- review activities. + Perform… more
- Henry Ford Health System (Southfield, MI)
- …informed consent processes, and human subjects protection principles. + Coordinate with the Institutional Review Board ( IRB ) to facilitate efficient ... Ford Health - Providence Hospital. The Director ensures compliance with institutional , regulatory, and ethical standards governing bothanimal and human subjects… more
- Texas A&M University System (Kingsville, TX)
- …University-Kingsville regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board ( IRB ), ... Duties and Responsibilities Regulatory Oversight & Review : + Coordinates the review and processing of research protocols for IRB (human subjects), IACUC… more
- University of Southern California (Los Angeles, CA)
- …research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board ( IRB ) and study sponsor. + ... documentation of study continuing review and study amendments to Institutional Review Board ( IRB ). Assists investigators with reportable event… more
- Cedars-Sinai (Beverly Hills, CA)
- …report forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board ( IRB ). The CRA I member ... long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …Subjects Protection Program in the areas of protocol reviews, liaison with the Institutional Review Board , and simple to moderately complex correspondence. ... **Minimum Qualifications/Work Experience:** 1+ years IRB experience. **Education/Licensure/Certification:** Bachelor's degree in a scientific or business discipline… more
- Cedars-Sinai (Beverly Hills, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). Primary Duties and ... study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious… more
- Cedars-Sinai (Beverly Hills, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… 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 & ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… 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 ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… more
- Cedars-Sinai (CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties & ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Job Duties and ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... participants. **5%** - Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB ), including the submission of Adverse… more