- AdventHealth (Orlando, FL)
- …agency requirements which govern the protection of human subjects in research . The IRB Specialist II conducts quality control functions for the IRB ... Specialist II provides training for IRB Office Coordinators, external IRB review...preferably in an academic or medical setting. + Certified Institutional Review Board Professional This… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Live Support, Clinical Research Operations Specialist II ...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… 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 ... for our superb clinical care and superior outcomes. The Research Grant Specialist II works...including, the Food and Drug Administration (FDA) and local Institutional Review Board . This position… 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 ... nationally for excellence in research !** The Clinical Research Data Specialist II manages...including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties… more
- University of Rochester (Rochester, NY)
- …analyze test data; prepare reports and make recommendations. Specifically, the research specialist will perform experiments involving cell purification, storage, ... Coordinate human blood draw and other sample collection with team of research clinical coordinators under IRB -approved protocols. Interface with Biological… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …and monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board ( IRB ) policies and ... trial portfolio. KEY RESPONSIBILITIES: + Assists regulatory team (Regulatory Specialist II and III) in research...to various review committees, including internal scientific review boards, the IRB and sponsoring entities.… more
- University of Rochester (Rochester, NY)
- …at The University of Rochester is seeking a part-time (20 hours/week) Human Subject Research Specialist , Level II , to coordinate human subject research ... activities. The division of Nephrology has a robust research portfolio that encompasses basic, translational, and clinical research . This individual would… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Regulatory Support Specialist II is responsible, for the coordination and oversight of regulatory requirements of ... Investigator (PI) and other study team members, the Clinical Research Regulatory Support Specialist II ...Research Manager. + Prepares and tracks/guides submission to IRB (CIRB, RSRB, Commercial IRB ), FDA, ClinicalTrials.gov,… more
- University of Rochester (Rochester, NY)
- …Critical Care, at The University of Rochester is seeking a full-time Human Subject Research Specialist , Level II , to coordinate human subject research ... activities. The division of Pulmonary Critical Care has a robust research portfolio that encompasses Pulmonary Arterial Hypertension, Lung Cancer Screening, Chronic… more
- UPMC (Pittsburgh, PA)
- …NDA-related activities; as well as other duties related to the documentation of research activities, review of the literature, preparation of progress reports, ... on investigating i) the effects of adolescent concussion on the developing brain, ii ) the extent to which these interfere with changes in pubertal hormones in… more
- University of Rochester (Rochester, NY)
- …at The University of Rochester is seeking a full-time Public Health Project Specialist II to coordinate the development and implementation of a federally ... funded lung cancer screening research project. Responsibilities include project management, overseeing data collection...the funding agency when necessary. + Develops and maintains IRB documentation (such as recruitment materials and data use… more
- Rush University Medical Center (Chicago, IL)
- …a billing plan for all medical procedures and services required in a clinical research project. * Review clinical research protocols and determine which ... consent form language. * Collaborate and communicate effectively with investigators and research staff, Patient Financial Services, the IRB , and Research… more
- Rush University Medical Center (Chicago, IL)
- …a billing plan for all medical procedures and services required in a clinical research project. * Review clinical research protocols and determine which ... consent form language. * Collaborate and communicate effectively with investigators and research staff, Patient Financial Services, the IRB , and Research… more
- University of Michigan (Dearborn, MI)
- …Teaching (25-40%) + Fulfill the position of Instructor of Record for ABA II Practicum, Behavioral Assessment Practicum, Research Methods in ABA Practicum ... instructor of record for the following methods courses: ABA II , Behavioral Assessment, & Research Methods +...and programmatic needs) fall, winter, and summer semesters + Research (5-10%) + Assist students with IRB … more
- Rush University Medical Center (Chicago, IL)
- …invoices from the vendors are received and accurate based upon agreed costs. * Review accuracy of the Clinical Research Coverage Analyst and Clinical Research ... Review / audit of daily activity of the Clinical Research Coverage Analyst and Clinical Research Financial...with Revenue Cycle colleagues, study teams, patients, Office of Research Affairs, IRB , RUMC Compliance, and all… more