- University of Southern California (Los Angeles, CA)
- …completion of some CRFs 6. Follows CISO SOPs II. Patient Care Related A. Physician/ Investigator Interaction 1 . Acts as consultant to PI in accruing patients. ... and Associate Director of CISO and to the Principal Investigator (s) with whom he/she works. This person is familiar...working. Specific Job Functions I. Research A. Protocol Related 1 . On request from supervisor, reviews new protocols prior… more
- Kelly Services (Irvine, CA)
- …R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones + Supports the clinical study team ... study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), and applicable trial registration on… more
- J&J Family of Companies (Irvine, CA)
- …Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Operating Company under ... (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports). + Supports applicable trial registration (eg… more
- Stanford University (Stanford, CA)
- … compliance . Regularly inspect study document to ensure ongoing regulatory compliance . + Work with principal investigator to ensure Investigational New ... States** Research Post Date Oct 10, 2025 Requisition # 107503 _This is a one ( 1 ) full-time (100% FTE), benefits-eligible, fixed term position for one ( 1 ) year.… 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
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** **Principal Investigator , Shouri Lahiri, MD is seeking for a motivated Research Associate III to join his team!** The Research Associate III ... and/or clinical activities, including but not limited to, budgetary/financial compliance , preparation of grant proposals, and creating independent presentations.… more
- The County of Los Angeles (Los Angeles, CA)
- …practices, policies and procedures, focusing on high-risk areas and its compliance to policies and procedures; determining whether internal controls are adequate ... audits and develops objectives to improve the efficiency, effectiveness, and/or compliance of the Sheriff Department's programs, operations, and records for… more
- Actalent (Palo Alto, 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 ... and management staff. + Interact regularly with the principal investigator to ensure patient safety and adherence to proper...a hybrid work environment with 4 days onsite and 1 potential flexible day. You will have the opportunity… more
- Bristol Myers Squibb (San Diego, CA)
- …support for IND preparation, regulatory authority interactions, design and execution of Phase 1 to Phase 3 clinical trials, and medical monitoring. This role works ... to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and… more
- Organon & Co. (Sacramento, CA)
- …and other internal stakeholders and direct FMDs appropriately within legal and compliance policies to implement medical strategies that support launch operating plan ... medical-to-medical materials, and conduct of research including facilitation of investigator -initiated trials as well as investigator selection, relationship… more