- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... ensure smooth coordination. + Assist with regulatory submissions to the Institutional Review Board (IRB), including Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Job Duties and Responsibilities:** ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions and respond to ... New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. + Managing the execution of… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **What are the Primary Duties & ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities + ... conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Beverly Hills, CA)
- …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **What are the Primary Duties and ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… 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 Responsibilities + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. _* - Other duties may… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board . **_*This position is hybrid*_** **Primary Duties ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Los Angeles, CA)
- …contact for long term follow-up patients only. Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising ... research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local… more
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