- University of Miami (Miami, FL)
- …a proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and Drug ... initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB...Federal , State and University policies regarding Humans Subjects Research and protection. Prepares specimens for submission to lab,… more
- Cedars-Sinai (Los Angeles, CA)
- …*Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... Clinical Research Associates. Ensures compliance with all federal , local, FDA, IRB , and HIPAA guidelines...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… more
- Cedars-Sinai (Los Angeles, CA)
- …Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... research billing. This role will comply with all federal , local, FDA, IRB , and HIPAA guidelines...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… more
- Johns Hopkins University (Fort Defiance, AZ)
- …and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific documentation ... and institutional policies pertaining to human subject's research and related matters. + Review applications...the FDA or commercial sponsors. + Assist in the review of IRB action outcomes, including the… more
- Stanford University (Stanford, CA)
- …manager, senior coordinator, and principal investigator. The CRCA will support industry, federal and grant funded clinical research studies. There are ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California,...the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... patient research billing. Ensures compliance with all federal , local, FDA, IRB , and HIPAA guidelines...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
- CUNY (New York, NY)
- …CUNY's Human Research Protection Program (HRPP), including oversight of Institutional Review Boards (IRBs); direct conflict of interest (COI) disclosure ... not be limited to the following: + Oversee convened IRB processes and meetings; review submissions; facilitate...conflict of interest, and oversight of social-behavioral and educational research . + Expert knowledge of federal regulations,… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... patient research billing. Ensures compliance with all federal , local, FDA, IRB , and HIPAA guidelines...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
- Cedars-Sinai (Beverly Hills, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... patient research billing. Ensures compliance with all federal , local, FDA, IRB , and HIPAA guidelines...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
- Cedars-Sinai (Los Angeles, CA)
- …contact for long term follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... patient research billing. Ensures compliance with all federal , local, FDA, IRB , and HIPAA guidelines...and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices… more