- Kaiser Permanente (Oakland, CA)
- Senior Manager, Research Compliance The Research ... research , research privacy, data management, Institutional Review Board ( IRB ) ... equivalent compliance certification. A CHRC (Certified in Healthcare Research Compliance ) is needed for this position Familiarity with regulatory agencies… more
- Kaiser Permanente (Oakland, CA)
- …those related to human subjects' research , research privacy, data management, Institutional Review Board ( IRB ) practices, and export controls. ... Compliance Consultant V - Research The Research Compliance ...and Food and Drug Administration (FDA). Demonstrated experience with Institutional Review Board ( IRB… 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 ... IRB and Advarra CIRB; prepare consent forms for research protocols. Prepare and submit application forms and serve... Review and Monitoring Committee, Joint Office of Compliance , Nursing Research Committee, Pathology Committee, and… more
- Kaiser Permanente (Vallejo, CA)
- …responsible for assisting in protecting the health, safety, and welfare of research participants. Essential Responsibilities: Compliance Support and comply with ... (Kaiser Permanente Code of Conduct). With guidance from PI, assist with ensuring compliance with KPNC IRB Standard Operating Procedures (SOP) and document… more
- Virginia Commonwealth University (Richmond, VA)
- …student research symposia. Familiarity with research compliance and institutional processes related to IRB review , responsible conduct of ... activities including funding and presentation opportunities. Assist students with Institutional Review Board ( IRB...collaborative relationships with institutional offices involved in research oversight, IRB , compliance , and… 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 ... closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB...Board duties, budgeting duties, and assisting with patient research billing and reconciliation. Ensures compliance with… more
- Planned Parenthood (Minneapolis, MN)
- … Research Manager. This position will focus on research study start-up, Institutional Review Board ( IRB ) submissions, study project coordination ... Day-to-Day Responsibilities: Study Coordination and Reporting Independently develop and prepare Institutional Review Board applications, including completion… more
- The University of Chicago (Chicago, IL)
- …and review process and when and how to apply for IRB review . Understanding of the federal research regulations and the ability to identify the federal ... deviations or violations, reports findings to PI, sponsor, and IRB under general direction of clinical research ... IRB approvals, and study related communication. Ensures compliance with federal regulations and institutional policies.… more
- The University of Miami (Miami, FL)
- …to research and strives to improve implementation and family outcomes. The Research Assistant 2 (A) ensures compliance with University policies, rules, and ... faculty or staff position using the Career worklet, please review this tip sheet. The University of Miami/UHealth Department...Ensure protocol is being followed as approved by the IRB . Participate in research activities by assisting… more
- Henry Ford Health System (Detroit, MI)
- …the established research protocol are met and in compliance with the Institutional Review Board ( IRB ) and sponsor guidelines. Identifies and ... Must have a minimum of 5 years of RN research experience. Experience managing the project IRB is a plus Clinical knowledge and analytical abilities necessary… more
- 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 ... of studies; develops and submits documentation and information for Institutional Review Board ( IRB...of physical and electronic data vulnerabilities; may develop or review research data security plans (RDSPs) for… more
- Tennessee Oncology (Chattanooga, TN)
- …and conducted in accordance with international, federal, state, and local regulations, and Institutional Review Board ( IRB ) approvals. This role ... clinical procedure and safety standards. ESSENTIAL FUNCTIONS: Manage day-to-day clinical research nursing operations, from protocol review /initiation to study… more
- Temple University (Philadelphia, PA)
- …and enter data; register subjects and study visits in OnCore; * Perform Epic research billing review ; * Maintain an up-to-date regulatory binder; * Schedule and ... Temple University's Clinical Research Department is searching for a Clinical ...attend sponsor visits; and prepare and submit IRB paperwork to ensure compliance with … more
- Piper Companies (Philadelphia, PA)
- …EKG, blood draws, Epic, OnCore, IRB submissions, regulatory binder, research billing review , subject enrollment, data collection, data entry, sponsor ... informed consent, regulatory compliance , clinical documentation, medication review , triage calls, clinical research experience, healthcare, medical… more
- Northwestern University (Chicago, IL)
- …local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration ... EXS/7 Job Summary Manages all activities associated with biomedical &/or social-behavioral research studies considered very complex by the inclusion of several of… more
- McInnis, Inc. (Ridgefield, CT)
- …experts, drive contract and budget negotiations (or amendments) with assigned sites; Review site-level documents needed for IRB /EC/REC approval; Support study ... The Clinical Research Associate will support clinical research ...and study monitoring plan; Ensure clinical study site documentation compliance according to GCPs, ICH and FDA regulations; Provide… more
- Stony Brook Medicine (Stony Brook, NY)
- …(IDE) applications. Creating Institutional Review Board ( IRB ) submissions and managing correspondence across research sites, particularly in single- ... this role contributes to the design, training, implementation, and regulatory compliance of research projects. Key responsibilities include creating and… more
- Northwestern University (Chicago, IL)
- …local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration ... of test data obtained in regard to biomedical &/or social-behavioral research study(ies) of limited complexity involving co-investigators, multiple campuses &/or… more
- Nuvance Health (Norwalk, CT)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... Clinical Research Coordinator, Norwalk, CT Full-time, 40 hours -...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… 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 ... deviation memos, physicians and coordinators' CVs and medical licenses, record of IRB certification and compliance ). Resolve regulatory related queries with … more
