- Primastep LLC (Arlington, VA)
- …and external partners with both federal and agency-specific human subject research regulations. Prepare and review Federalwide Assurances (FWAs) and DoD ... Qualifications: Completion of CITI training in Human Subjects Research or IRB Administration. Prior experience supporting military or federal human … 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. ... care for kids in California. Here world-class experts in medicine, education and research work together to deliver family-centered care half a million times each… more
- WCG Clinical (Cary, NC)
- …of documents, client reporting and problem resolution. This position will: + Support the Board and clients by preparing documents for review in accordance with ... WCG IRB Operations Specialist (Remote) **General Information** **Organization:** WCG...+ Knowledge of FDA regulations as they relate to research (preferred) + Must be able to maintain confidentiality… more
- Primastep LLC (Arlington, VA)
- …Arlington, VA. This role ensures the protection of human subjects involved in research activities by maintaining compliance with federal and Department of ... DON IRB -approved studies. Regulatory Documentation & Assurance Packages Prepare, review , and submit Federalwide Assurance (FWA) and DoD Assurance packages for… more
- Stony Brook University (Stony Brook, NY)
- … (ie Cerner Powerchart). Experience working with an IRB (Investigational Review Board ) for research protocol submissions, amendments and reviews. ... correspond with various internal and external constituents including sponsors, cooperative groups, Institutional Review Board and regulatory agencies. + May… more
- Stony Brook University (Stony Brook, NY)
- …Act (HIPAA) and institutional regulations (eg, regulations pertaining to the Institutional Review Board ( IRB ). Demonstrated knowledge of ... Data Use Agreement Manager reports to the Director for Research Security in the Office of Research ...end-to-end process for data sharing related agreements including initial review of agreement and IRB submission/approval, negotiation,… more
- Stony Brook University (Stony Brook, NY)
- …duties: + Review all active protocols, manage clinical trials from IRB initiation to close-out. + Sponsor's monitoring visits, and responsible for drug/device ... Clinical Research Associate I **Required Qualifications (as evidenced by...+ Submit pharmaceutical proposals and consent forms to the IRB . + Liaison between SBMC, pharmaceutical sponsor, patient and… more
- Jobleads-US (Sunnyvale, CA)
- …to research conducted by 23andMe which is overseen by an independent third-party Institutional Review Board ( IRB ) regulated under the Common Rule ... Overview We are a group of individuals passionate about genetic discovery. 23andMe Research Institute is a nonprofit medical research organization that enables… more
- Stony Brook University (Stony Brook, NY)
- …Oncology/Chemotherapy experience. Research experience coordinating clinical trials and IRB research training. **Special Notes** **:** **Resume/CV should be ... Research Nurse - Cancer Clinical Trials **Position Summary**...patient eligibility for protocol participation by way of chart review , data collection and patient evaluation/assessment identification. In addition,… more
- Florida Atlantic University (Davie, FL)
- …collaborators. Responsibilities: + Review , redline, and negotiate externally funded research agreements and terms from federal , state, foundation, and local ... agreements and outgoing subawards. The administrator ensures compliance with federal , state, foundation, and institutional requirements, while facilitating… more
- Stony Brook University (Stony Brook, NY)
- …discussing study protocol. + Documenting research encounters. + Communicating with the Institutional Revenue Board ( IRB ) and the study team. + Other ... or higher) in Psychology, Healthcare, Neuroscience, Biology or related field. Research experience. Experience in a Clinical Setting. Experience with patients.… more
- Stanford Health Care (Palo Alto, CA)
- …Provides the full range of distributive, clinical, consultative, research , investigational, and/or administrative pharmaceutical services. Incumbents select, ... hospital staff and interested community groups; may participate in hospital research projects or perform pharmaceutical research . **Locations** Stanford Health… more
- University of Utah (Salt Lake City, UT)
- …and regulatory issues associated with human research protections and compliance for the Institutional Review Board ( IRB ). Provides direct ... Details **Open Date** 10/24/2025 **Requisition Number** PRN43397B **Job Title** Institutional Review Board Adm **Working...human research protections and IRB review processes for IRB employees, board… more
- Huron Consulting Group (Van Buren, AR)
- …concurrently and apply your expertise and work ethic to process and review Institutional Review Board ( IRB ) submissions and conflict of interest ... and other individuals) and COI disclosures. + Conducts pre- review of IRB submissions to determine federal agency oversight, evaluate for missing materials,… 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 ... the institution's academic mission. Performance Expectations: + Maintain full compliance with institutional and federal research regulations. + Demonstrate… more
- HonorHealth (AZ)
- …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... the IRB Coordinator facilitates initial and continuing review of research protocols in compliance with...This includes initial determinations regarding expedited, exempt, or full board review , as well as human subject… more
- Mount Sinai Health System (New York, NY)
- …events in accordance with MSSM Institutional Review Board ( IRB ) SOPs, sponsor guidelines, and federal regulations + Assist the PI and regulatory ... research . + Working knowledge Good Clinical Practice guidelines and Federal research regulations. + Demonstrate strong organizational and communication… more
- Sam Houston State University (Huntsville, TX)
- …procedures in accordance with Institutional Review Board ( IRB )-approved protocols. Collects and enter clinical research data with accuracy and ... recruitment, informed consent, and data collection activities while ensuring compliance with institutional and federal research regulations. Develops and… more
- Texas State University (San Marcos, TX)
- … research administration, law, public policy, science, or ethics) + Federal Research Regulations: Comprehensive understanding of laws, policies, and guidance ... governing: + Human subjects research (Common Rule, IRB... Misconduct ( ORI standards) + Responsible Conduct of Research ( RCR training mandates) + Institutional … more
- Novant Health (Charlotte, NC)
- …will establish governance structures, implement process improvements, and ensure adherence to federal research regulations, including IRB and human subjects' ... What We Offer The Vice President (VP) of Research and Innovation is a senior leader responsible for driving Novant Health's strategic research initiatives,… more
