- Pfizer (South San Francisco, CA)
- …and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation of clinical study results + Support execution ... and interpretation of clinical trials data together with the GDL, Clinical Safety , and Biostatistics. + Serve as technical resource for clinical issues raised… more
- J&J Family of Companies (Irvine, CA)
- …(eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports); + Ensures applicable trial registration (eg on ... + Oversees and supports the development and execution of Investigator agreements and trial payments. + Is responsible for...while maintaining optimal efficiency. + May act as Clinical Safety Coordinator. + May perform other duties assigned as… more
- Stanford University (Stanford, CA)
- …define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study ... study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA… more
- Stanford University (Stanford, CA)
- …define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study ... study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA… more
- Stanford University (Stanford, CA)
- …status. **In this role, you will** **:** + Participate with principal investigator in the preparation of the administrative components of proposals within parameters ... Serve as a subject matter expert and overall technical resource to principal investigator and other university staff. + Participate in and contribute to process… more
- Stanford University (Stanford, CA)
- …define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study ... study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA… more
- Stanford University (Stanford, CA)
- …campus but is remote eligible. **Duties include:** + Participate with principal investigator in the preparation of the administrative components of proposals within ... resource on subject area and overall technical resource to principal investigator and other university staff. **DESIRED QUALIFICATIONS:** + Higher Education… more
- Stanford University (Stanford, CA)
- …projects, and federal awards. **CORE DUTIES** **:** + Participate with principal investigator in the preparation of the administrative components of proposals within ... as a resource on subject area and overall technical resource to principal investigator and other university staff. + Participate in and contribute to process… more
- Stanford University (Stanford, CA)
- …define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study ... study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA… more
- Stanford University (Stanford, CA)
- …define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study ... study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA… more