- 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 (Fixed-term 12 months)...documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review… 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 (1 Year Fixed-Term)...documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review… more
- Johns Hopkins University (Baltimore, MD)
- …and Director of the Medical Intensive Care Unit (ICU) is seeking a **_Sr. Research Program Coordinator II_** who will have duties and responsibilities related to ... laboratory manuals. + Internally monitor regulatory files and study data to assess compliance , data quality, and accuracy. + Complete IRB amendment submissions… 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 (Hybrid Opportunity) **School of...documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Monitor ... Research Coordinator & Lab Manager @...documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review… 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,...documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review… 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,...of interview, focus group and other data. * Ensure compliance with research protocols, and review… more
- Johns Hopkins University (Baltimore, MD)
- …etc.). Edit and complete IRB submissions, including new projects, continuing review , change in research , termination reports, and further study actions. + ... databases (OnCore, REDCap, Openspecimen, iLabs). + Ensure adherence to study protocols ( IRB compliance ) and study quality and maintain patient confidentiality. +… more
- Beth Israel Lahey Health (Burlington, MA)
- … duties. Implements study protocols in accordance to regulatory and institutional requirements. Works closely with principal investigators, research staff ... applicable. + Attends Investigator Meetings as applicable. 4) Conducts assigned research studies per protocol requirements, departmental and institutional … more
- Guthrie (Sayre, PA)
- …total research department. Other Duties: + Collaborate with executive director, manager, research team members and IRB coordinator in developing and ... Responsibilities for program development include assisting with feasibility, site selection, IRB document review , and corresponding with investigators, IRB… more