- 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 Coordinator Associate (1 Year Fixed-Term) **School of Medicine,...of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits… 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 Coordinator Associate **School of Medicine, Stanford, California, United...of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits… 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 Coordinator Associate **School of Medicine, Stanford, California, United...of patient and research data in appropriate files per institutional and regulatory requirements. * Participate in monitor visits… more
- Actalent (Los Angeles, CA)
- Clinical Research Coordinator - Relocate to Merced, CAJob Description We are seeking an experienced Clinical Research Coordinator with a minimum of 3 years of ... alongside a nurse lead. Responsibilities + Perform regulatory tasks, including IRB submissions. + Engage in sponsor correspondence, excluding budget and contracting.… more
- General Dynamics Information Technology (Camp Pendleton, CA)
- …of clinical protocols, consent forms and other documents to the scientific review committee, IRB and other regulatory organizations.** **Prepares requests for ... Required:** NACLC (T3) **Job Family:** Research **Skills:** Clinical Research,Informed Consent, IRB (Inactive),Participant Recruiting **Experience:** 3 + years of related… more
- Actalent (Merced, CA)
- Job Title: Clinical Research Coordinator Job Description We are seeking a Clinical Research Coordinator with a minimum of 3 years of clinical research ... with a nurse lead. Responsibilities + Perform regulatory tasks, such as IRB submissions. + Maintain sponsor correspondence, excluding budget and contracting. +… 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 Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to coordinate...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 ... Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to coordinate...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 ... and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical… more
- University of Southern California (Los Angeles, CA)
- …Coordinator IApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Research- Coordinator -I\_REQ20164274/apply) Keck ... interest in clinical research. The role of the Research Coordinator I is a diverse one. This person works...Events. Enters SAE into iStar for reporting to the IRB . Notifies Data Managers promptly of occurrence of SAE.… more