- University of Florida (Gainesville, FL)
- … Specialist II Apply now (https://secure.dc4.pageuppeople.com/apply/674/gateway/default.aspx?c=apply&lJobID=532161&lJobSourceTypeID=796&sLanguage=en-us) Job ... Department: 29070100 - MD-OBSTETRICS / GYNECOLOGY-GEN Classification Title: Administrative Specialist II Job Description: The Administrative Specialist… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties and Responsibilities** + May ... nationally for excellence in research!** The Clinical Research Data Specialist II manages the data for assigned...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Cedars-Sinai (Los Angeles, CA)
- …local agency requirements, including, the Food and Drug Administration (FDA) and local Institutional Review Board . This position is hybrid **Primary Duties ... superb clinical care and superior outcomes. The Research Grant Specialist II works with Principal Investigator to...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Mount Sinai Health System (New York, NY)
- …to the appropriate committee ( Institutional Animal Care and Use Committee, Institutional Review Board , Bio-Safety Officer and Financial Conflict of ... experience. + Clinical trials negotiation training (MAGI, etc.) desirable. + Certified IRB Professional (CIP): Active Certification -- or Eligibility to take the… more
- University of Rochester (Rochester, NY)
- …at The University of Rochester is seeking a full-time Human Subject Research Specialist , Level II , to coordinate human subject research activities. The division ... data management, interactions with subjects and communication with regulators (eg CRO, IRB ). The coordinator will also provide cross-coverage of other trials in the… more
- University of Rochester (Rochester, NY)
- …University of Rochester is seeking a part-time (20 hours/week) Human Subject Research Specialist , Level II , to coordinate human subject research activities. The ... recruitment strategies, information, data systems and study management systems; development, review and approval of case report forms (CRFs) and study-specific… more
- Methodist Health System (Dallas, TX)
- …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and… more
- Childrens Hospital of The King's Daughters (Norfolk, VA)
- …+ Performs other duties as assigned. + LICENSES AND/OR CERTIFICATIONS + Completion of IRB ( Institutional Review Board ) certification in human subjects' ... + Increased Security Clearance Required for Job Roles in Medical Tower II : FBI fingerprinting, criminal background check, and Child Protective Services registry… more
- Rush University Medical Center (Chicago, IL)
- …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents to prepare a billing plan ... and services required in a clinical research project. * Review clinical research protocols and determine which procedures are...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB… more
- Rush University Medical Center (Chicago, IL)
- …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents in order to prepare a ... and services required in a clinical research project. * Review clinical research protocols and determine which procedures are...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB… more