- Stanford University (Stanford, CA)
- …the development phase, including draft content and formatting to meet requirements of Stanford, Institutional Review Board ( IRB ), United States Food and ... research setting. + Strong knowledge of regulatory affairs, including FDA regulations, IRB review and approval process, and Good Clinical Practice. +… more
- Houston Methodist (Houston, TX)
- …regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the...and applicable regulations. + Assists in the preparation of research protocols for IRB submission, submitting protocol… more
- University of Pennsylvania (Philadelphia, PA)
- …(including continuing reviews, amendments, and adverse event reporting) to the University of Pennsylvania Institutional Review Board ( IRB ). + Assist in ... private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among… more
- Baylor Scott & White Health (Plano, TX)
- …and exclusion criteria are met. + Partners and coordinates with regulatory compliance. Prepares Institutional Review Board ( IRB ) materials for protocol ... clinical trials. This includes all trial phases, from pre-study to closure, following federal , state, and Institutional guidelines. This position will learn to… more
- Mount Sinai Health System (New York, NY)
- …grant applications and documents and assists in protocol submissions (for eg, Institutional Review Board , Grants and Contracts Office). **Qualifications** ... and innovative community based programs. Under minimal supervision, the Clinical Research Coordinator II coordinates the clinical assessments of the study subjects;… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... Full time Scheduled Weekly Hours: 40 Department: 400153 OBGYN Research Work Shift: UR - Day (United States of...and close out visits. + Keeps current with all federal , state, sponsor, and institutional policies and… more
- Mayo Clinic (Rochester, MN)
- …and verification of content to meet institutional and federal standards; Institutional Review Board ( IRB ) submission; and communication with ... the Rochester, MN campus.** Coordinates non-therapeutic (ie minimal risk, survey, chart review ) clinical research protocols with direction from the principal… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... inspection, initiation, on-going and close out visits). - Keeps current with all federal , state, sponsor, and institutional policies and laws, standard operating… more
- Mount Sinai Health System (New York, NY)
- …organization of study information. Assists in preparing grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office), and ... **Job Description** The Clinical Research Assistant I assists in the daily activities...information into database. + Assists in preparing grant applications, IRB /GCO for submission and filings. + Maintains source documents… more
- Cedars-Sinai (Los Angeles, CA)
- …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical ... **Job Description** **Join us as a Research Grant Specialist II (RGS II) as we...including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Job… more