- Cedars-Sinai (Los Angeles, CA)
- …patient contact for long term follow-up patients only. Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with ... research data, and assist with regulatory submissions to the IRB . Provides limited patient contact as needed for study...supervising research staff or directly with the Institutional Review Board to submit… 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 ... research data, and assist with regulatory submissions to the IRB . Provides limited patient contact as needed for study...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… 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 ... research data, and assist with regulatory submissions to the IRB . Provides limited patient contact as needed for study...including the Food and Drug Administration (FDA) and local Institutional Review Board . *Maintains research… more
- Cedars-Sinai (Los Angeles, CA)
- …and study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... local agencies including the Food and Drug Administration (FDA and local Institutional Review Board . **Primary Duties and Responsibilities:** + Scheduling of… more
- Cedars-Sinai (Los Angeles, CA)
- …and study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... local agencies including the Food and Drug Administration (FDA and local Institutional Review Board . **_*This position is hybrid*_** **Primary Duties and… more
- Cedars-Sinai (Los Angeles, CA)
- …term follow-up patients only. + Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices using Good Clinical… more
- CommonSpirit Health (Santa Maria, CA)
- …study/regulatory, documents, applications and forms, including but not limited to the applicable Institutional Review Board ( IRB ) application form(s), ... as well as protocol deviations, violations or exceptions, to the study sponsor and IRB as required by GCP, FDA, OHRP and CommonSpirit Health policy. + In conjunction… more
- Cedars-Sinai (Beverly Hills, CA)
- …trial budget. + Performs Medicare coverage analysis for clinical trials and collaborates with Institutional Review Board ( IRB ) to finalize and obtain ... agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties and Responsibilities:** + Works closely… more
- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations;… more