- The University of Chicago (Chicago, IL)
- …submission and review process and when and how to apply for IRB review . Understanding of the federal research regulations and the ability to identify ... deviations or violations, reports findings to PI, sponsor, and IRB under general direction of clinical research ...the federal research organizations' role in regulating human research … more
- Northwestern University (Chicago, IL)
- …& federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration (FDA) ... Ensures that all study documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols are completed… more
- Northwestern University (Chicago, IL)
- …& federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration (FDA) ... scientific papers. Completes documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols. Finance… more
- Cedars Sinai (Beverly Hills, CA)
- … 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...research billing and reconciliation. Ensures compliance with all federal and local agencies including the Food and Drug… 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
- 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 ... private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among… more
- University of Massachusetts Medical School (Worcester, MA)
- … related supplies Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board ( IRB ) processes Provide ... services, and prevention practices. Responsibilities ESSENTIAL FUNCTIONS: Obtain consent of research participants in accordance with the IRB approved protocols… more
- BayCare Health System (Tampa, FL)
- …with the standards of good clinical practice, federal and state regulations and institutional review board ( IRB ) requirements Ensures adherence to ... of trust, dignity, respect, responsibility, and clinical excellence. Title: Clinical Research Nurse I - Oncology Facility: St. Joseph's Hospital Responsibilities:… more
- Children's National Hospital (Washington, DC)
- …of action plans to improve quality. Facilitates the preparation of Institutional Review Board applications for research proposals, develops and manages ... and manage research and/or research intervention projects within the federal and institutional regulations and policies under the direction of the… more
- The University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... team members in retrieval and provision of documentation required for IRB submission/renewals in accordance with guidelines; continuing review , modification,… more
- Mount Sinai Hospital (New York, NY)
- …grant applications and documents and assists in protocol submissions (for eg, Institutional Review Board , Grants and Contracts Office). Responsibilities ... 1. Analyzes moderately complex clinical research data; Assists in interpreting clinical research ...the study subjects. 3. Prepares and ensures grant applications, IRB /GCO documents are submitted. 4. Ensures accurate and complete… more
- Tennessee Oncology (Chattanooga, TN)
- …conducted in accordance with international, federal , state, and local regulations, and Institutional Review Board ( IRB ) approvals. This role involves ... clinical procedure and safety standards. ESSENTIAL FUNCTIONS: Manage day-to-day clinical research nursing operations, from protocol review /initiation to study… more
- CHOC - Children's Health Orange County (Orange, CA)
- …protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board ( IRB ), identifying potential study ... CHOC can take you. Job Summary With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple… more
- Northwestern University (Chicago, IL)
- …& federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration (FDA) ... of test data obtained in regard to biomedical &/or social-behavioral research study(ies) of limited complexity involving co-investigators, multiple campuses &/or… more
- Stony Brook Medicine (Stony Brook, NY)
- …(IDE) applications. Creating Institutional Review Board ( IRB ) submissions and managing correspondence across research sites, particularly in single- ... IRB /multi-site studies. Planning and implementing changes to the research plan in collaboration with the PI and study team. Collaborating with investigators and… more
- The University of Miami (Miami, FL)
- …maintains source documentation. Ensure protocol is being followed as approved by the IRB . Participate in research activities by assisting in the collection of ... 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
- Kaiser Permanente (Vallejo, CA)
- …process by coordinating the current consent documents. According to protocol and/or IRB -approved telephone script, collect and document research data in a ... Job Summary: The Clinical Trial Research Coordinator I (CTRC-I) is a novice level...an ongoing basis. If applicable and with supervision, coordinate IRB communications (eg, new protocols, amendments, continuing review… more
- The University of Pennsylvania (Philadelphia, PA)
- …and experience with administering cognitive assessments strongly preferred. Familiarity with IRB guidelines, human subject research practices, and appropriate ... private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among… more
- Holy Cross Hospital (Fort Lauderdale, FL)
- …person will be responsible for the conduct of multiple Oncology clinical research activities. Ideal candidate will have industry sponsored clinical trial experience. ... maintaining up to date knowledge on these policies from IRB , FDA, ICH, GCP, or other sources *FL RN...or other sources *FL RN License *On-Site *Oncology Experience * Research Experience What you will do: Assist in the… more
