- Cedars-Sinai (Los Angeles, CA)
- …long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... report forms, entering clinical research data, and assist with regulatory submissions to the IRB . Provides limited...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Cedars-Sinai (Los Angeles, CA)
- …long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... report forms, entering clinical research data, and assist with regulatory submissions to the IRB . Provides limited...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Cedars-Sinai (Los Angeles, CA)
- …long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... report forms, entering clinical research data, and assist with regulatory submissions to the IRB . Provides limited...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… 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 ... report forms, entering clinical research data, and assist with regulatory submissions to the IRB . Provides limited...including the Food and Drug Administration (FDA) and local Institutional Review Board . *Maintains research… 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 ... Safety Letters following local and federal guidelines. + May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting… 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 ... Safety Letters following local and federal guidelines. + May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting… more
- Cedars-Sinai (Los Angeles, CA)
- …patients only. + Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... 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)
- …, documents, applications and forms, including but not limited to the applicable Institutional Review Board ( IRB ) application form(s), informed ... and clinical trials processes required. + Experience in preparing and maintaining regulatory documents and other IRB -related study documentation required. + Lab… more
- Stanford University (Stanford, CA)
- …and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble study ... documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and … 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 ... federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good… more