- 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices… 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 ... data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities,...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… more
- Cedars-Sinai (Santa Monica, CA)
- … staff meetings. + Works closely with investigators and regulatory staff or directly with Institutional Review Board ( IRB ) to submit adverse events, ... professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements.… more
- Cedars-Sinai (Los Angeles, CA)
- … staff meetings. + Works closely with investigators and regulatory staff or directly with Institutional Review Board ( IRB ) to submit adverse events, ... professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements.… 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 ... smooth coordination. + Assist with regulatory submissions to the Institutional Review Board ( IRB...Board duties, budgeting duties, and assisting with patient research billing and reconciliation. + Ensures compliance … 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 ... closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB...Board duties, budgeting duties, and assisting with patient research billing and reconciliation. + Ensures compliance … 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 ... and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... . Responsibilities include preparation of initial study documents for IRB submission in compliance with all local,...documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review… more
- Stanford University (Stanford, CA)
- …strategies for recruitment, data quality control procedures and processes). May follow up with Institutional Review Board ( IRB ) to ensure renewals are ... studies. There is potential for working with human subjects research and will need to assist with IRB...for completion and accuracy with source documents and ensure compliance with research protocols. + Identify, select,… 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 ... and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol...billing. This role will follow all federal, local, FDA, IRB , and HIPAA guidelines and regulations pertaining to the… more