- University of Pennsylvania (Philadelphia, PA)
- … B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB ... more
- Cedars-Sinai (Beverly Hills, CA)
- …study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Cedars-Sinai (Beverly Hills, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- 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 ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Cedars-Sinai (Los Angeles, CA)
- …activities. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Johns Hopkins University (Baltimore, MD)
- …through recruiting and enrolling eligible patients into studies. + Prepare relevant documents for Institutional Review Board and as well for EPIC tracking. + ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. *Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... more
- Actalent (Philadelphia, PA)
- …process, documenting adverse events, and collecting study documents. This role requires preparing Institutional Review Board ( IRB ) applications and ... more
- UCLA Health (Los Angeles, CA)
- …documents, and all required applications and forms + submissions to the applicable Institutional Review Board ( IRB ), informed consent form ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- University of Pennsylvania (Philadelphia, PA)
- …data entry. Independently manage different phases of clinical trials. They may assist with Institutional Review Board ( IRB ) filings, sponsor and ... more
- Nuvance Health (Danbury, CT)
- …patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... more
- Johns Hopkins University (Baltimore, MD)
- … IRB requirements, and facilitates IRB audits. + Interacts with Johns Hopkins Institutional Review Board and staff. + Enters e- irb protocols and ... more
- Nuvance Health (Poughkeepsie, NY)
- …patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... more
- Nuvance Health (Norwalk, CT)
- …patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... more
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