- Stanford University (Stanford, CA)
- …both routine and complex. **Duties include:** + Participate with principal investigator in the preparation of the administrative components of proposals within ... submission process, both paper and electronic; review documents for completeness and compliance . + Develop, prepare, and finalize project budgets, and provide budget… more
- Actalent (Merced, CA)
- …develop flow sheets, and complete study documents/case report forms. + Ensure compliance with research protocols and review/audit case report forms for accuracy with ... with finance and management staff. + Interact regularly with the principal investigator to ensure patient safety and adherence to proper study conduct. +… more
- Parexel (Sacramento, CA)
- …solutions. As a member of this team, you will be essential to ensuring our Investigator sites are prepared to start trials, with a focus on reducing Site Activation ... + Collects and reviews initial regulatory packets and site contracts for investigator sites. + Coordinate efforts for all site activation related activities… more
- Bristol Myers Squibb (San Diego, CA)
- …of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial ... and regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Establish and maintain… more
- Stanford University (Stanford, CA)
- …funds, personnel, and equipment as needed. Coordinate and collaborate with principal investigator to review study protocol and assess and analyze feasibility, budget ... Administration, National Institutes of Health, etc.). + Support sponsor investigator research with Investigational New Drug/Investigational Device Exemption applications.… more
- Bristol Myers Squibb (San Diego, CA)
- …to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and ... regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Establish and maintain… more
- BeOne Medicines (San Mateo, CA)
- …affairs, clinical development, program leadership, clinical operations, legal, compliance , new product planning, clinical business development intelligence, ... clinically relevant regional medical meetings (eg, advisory boards, consultant, and investigator meetings), as requested + Build strong relationships with internal… more
- Stanford University (Stanford, CA)
- …regulations. The CRCA will work under close direction of the principal investigator and study managers/supervisors as well as work collaboratively with research ... study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case report forms for… more
- Cordis (Irvine, CA)
- …activities to ensure adherence to appropriate industry US and OUS regulations, compliance with the study Protocol(s), and applicable local regulations + Assist in ... are of a high quality + Assist with organization and preparation for Investigator meetings and Study Coordinator meetings + Ensure proper escalation of site/project… more
- Stanford University (Stanford, CA)
- …clinical studies and work under close direction of the principal investigator and/or study coordinator/supervisor. **Duties include:** + Serve as primary contact ... other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols and review and audit case report forms for… more