- Genentech (South San Francisco, CA)
- …at maximizing medical progress, while serving as the guardian for high standards of compliance , ethics, and safety. They will play a critical role to establish and ... execution of high quality Phase IIIb/IV clinical trials and investigator -initiated research including study design, protocol writing, approval, implementation and… more
- Cedars-Sinai (CA)
- …and/or clinical activities, including but not limited to, budgetary/financial compliance , preparation of grant proposals, and creating independent presentations. Not ... troubleshooting, etc.). Organizes clinical/research trials in conjunction with the Principal Investigator and sponsor and/or funding source. Monitors and ensures … more
- AbbVie (Irvine, CA)
- …+ Based on strong medical and scientific experience, knowledge of compliance and regulatory requirements, Allergan Aesthetics customers, markets, business operations ... design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers,… more
- Genentech (South San Francisco, CA)
- …an enterprise mindset. They serve as the guardian for high standards of compliance , ethics and safety. **Key Responsibilities** **Who you are** + Co-own with the ... execution of high quality Phase IIIb/IV clinical trials and investigator -initiated research including study design, protocol writing, approval, implementation and… more
- BeOne Medicines (Emeryville, CA)
- …Affairs, clinical development, program leadership, clinical operations, legal, compliance , new product planning, clinical business development intelligence, US ... execution of regional medical meetings (eg, advisory boards, consultant, and investigator meetings), as requested + Build strong relationships with internal experts… more
- Bristol Myers Squibb (Los Angeles, CA)
- …TLs/HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives. + Actively ... partner with HCPs on disease state initiatives, collaborative research projects, and investigator sponsored research (ISR) of interest and in alignment with BMS… more
- Stanford University (Stanford, CA)
- …study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case report forms for ... with finance and/or management staff. + Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.… more
- J&J Family of Companies (Irvine, CA)
- …(CSER) Team responsible for global evidence dissemination of scientific findings from investigator led clinical trials and registries sponsored by Johnson & Johnson ... study protocols and clinical study reports, ensuring scientific soundness and compliance with regulatory requirements + Conducts literature & landscape reviews to… more
- Pfizer (San Diego County, CA)
- …and regulatory activities including product labels, core data sheets, Investigator Brochures, Development Safety Update Reports, and Periodic Benefit-Risk Evaluation ... support (DSUR, PBRER) submission disclosure deliverables and product defense. + Ensures compliance with internal SOPs and external regulatory standards. + Review IIR… more
- UCLA Health (San Luis Obispo, CA)
- …multicenter clinical trials (both NIH and industry-sponsored), local investigator -initiated clinical trials, and/or programmatic clinical research activities. ... as needed to support and provide guidance on the administration of the compliance , financial, personnel and other related aspects of studies. Annual salary range:… more