- Stanford University (Stanford, CA)
- …administer sponsored projects. + Demonstrated understanding of terminology, such as compliance , title, sub-contractor, consultant, audit , and accounting review. ... Research Administrator 1 **School of Medicine, Stanford, California, United States** **New** Finance Post Date 5 days ago Requisition # 106942 The Department of… more
- Stanford University (Stanford, CA)
- …other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case report ... Clinical Research Coordinator Associate ( 1 Year Fixed-Term) **School of Medicine, Redwood City,...clinical data and research samples as well as ensuring compliance and safety under the supervision of the principal… more
- Stanford University (Stanford, CA)
- Social Science Research Professional 1 , General Surgery (Hybrid Opportunity) **School of Medicine, Stanford, California, United States** Research Post Date Mar 19, ... Stanford University is seeking a Social Science Research Professional 1 to perform work to support research or develop...+ Analyze and summarize results for review with supervisor. Audit the accuracy and validity of data. + Review… more
- University of Southern California (San Diego, CA)
- …will include, but are not limited to: + Participate with principal investigator in the preparation of the administrative components of proposals within parameters ... process, both paper and electronic. Reviews documents for completeness and compliance . + Develop, prepare, and finalize project budgets. Provide budget… more
- Stanford University (Stanford, CA)
- …other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case report ... Lab Manager working remotely and required to go on-site 1 day or less per week. This position will...calendar and coordinate meetings. + Interact with the principal investigator regularly, + Ensure essential documentation of research data… more
- Cordis (Irvine, CA)
- …Ensures accuracy, validity, and completeness of data at trial sites in compliance with the protocol, clinical monitoring plan, informed consents forms and associated ... and associated training documentation is available in the site's investigator file and sponsor trial master file + Contribute...into trial activities, such as trends in enrollment, protocol compliance , and data quality. Escalate site issues to the… more