- Stanford University (Stanford, CA)
- …resolve study queries. + 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)
- …do not exist. General instruction provided by the supervisor or principal investigator . May interpret study results in collaboration with supervisor or PI. + ... conceptual approach. + Build and organize data as requested by principal investigator or supervisor; use common statistical programs requiring the application of job… more
- Stanford University (Stanford, CA)
- …contact for students, residents, and fellows working with the principal investigator . The candidate will maintain an active database of ongoing ... conceptual approach. + Build and organize data as requested by principal investigator or supervisor; use common statistical programs requiring the application of job… 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
- J&J Family of Companies (Irvine, CA)
- …(eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports, ); + Supports applicable trial registration (eg ... + Oversees and supports the development and execution of Investigator agreements and trial payments; + Is responsible for...Supports project/study budget activities; + May act as Clinical Safety Coordinator (See ANNEX I - Clinical Safety… more
- Sanofi Group (Sacramento, CA)
- …Development, Regulatory, etc. to facilitate diligence reviews, medical and safety evaluation, product positioning, lifecycle evidence planning, and compliance needs. ... and identifying opportunities for further data collection clinical or investigator -led** + Monitors disease epidemiology and provides support, including protocol… more
- Sumitomo Pharma (Sacramento, CA)
- …interacting with CROs, medical monitors, and vendors as required, and working with the safety group to ensure adequacy of safety monitoring and reporting + ... writing of clinical study reports + Contributes to the preparation of Investigator Brochures, annual reports, data collection systems and final reports in compliance… more
- J&J Family of Companies (Irvine, CA)
- …(eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports) with minimal direction. + Ensure trial registration ... + Lead all aspects of development and execution of Investigator agreements and trial payments. + Leads clinical data...Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable + For those… more
- Cedars-Sinai (Los Angeles, CA)
- …but in close cooperation and in consultation with the Principal Investigator . The Postdoctoral Scientist will perform routine and complex laboratory procedures ... records and documentation and analyze the results with the Principal Investigator May develop, adapt, and implement new research techniques and protocols.… more