- BeOne Medicines (Emeryville, CA)
- …answer ad-hoc safety queries from ethics committees. + Lead the authoring and review of safety sections of regulatory submissions, eg, IND/CTA (General ... execution, communication and influence with internal stakeholders (eg, clinical development, medical , regulatory , labeling) and external stakeholders (eg FDA,… more
- Bristol Myers Squibb (San Diego, CA)
- …+ Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents + Conduct ... aims to be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has responsibility for the… more
- Cedars-Sinai (Marina Del Rey, CA)
- …+ One (1) to two (2) years of experience in quality improvement, regulatory compliance , or performance improvement, with a strong preference for candidates ... limited to Core Measures, Patient Safety Indicators (PSI-90), and Mortality review processes, to ensure sustained optimal performance. The Patient Safety Specialist… more
- Sumitomo Pharma (Sacramento, CA)
- …Initiated Study and Collaborative Research program. + Provide detailed and compliant medical review and approval of external resources, communications, and ... track record of detailed, medically accurate, and scientifically relevant writing and review skills in line with compliance requirements. + Experience… more
- BeOne Medicines (San Mateo, CA)
- …answer ad-hoc safety queries from ethics committees + Lead the authoring and review of safety sections of regulatory submissions, eg, IND/CTA (General ... execution, communication and influence with internal stakeholders (eg, clinical development, medical , regulatory , labeling) and external stakeholders (eg FDA,… more
- Veterans Affairs, Veterans Health Administration (Los Angeles, CA)
- …changes in policies or procedures. iv. Ability to determine and evaluate compliance with legal, ethical, and regulatory guidelines, and accrediting bodies ... improvement, records management, release of information, file room/scanning, transcription and medical speech recognition, as well as the overall management of… more
- HCA Healthcare (Riverside, CA)
- …will monitor and maintain credential files to ensure completeness and accuracy; review all file documentation for compliance with quality standards, ... satisfaction and personal growth, we encourage you to apply for our Medical Staff Credentialing Coordinator opening. We promptly review all applications.… more
- Evolent (Sacramento, CA)
- …when available, within the regulatory timeframe of the request. + Utilizes medical /clinical review guidelines and parameters to assure consistency in the MD ... culture. **What You'll Be Doing:** As a Cardiology, Field Medical Director you will be a key member of...review process to reflect appropriate utilization and … more
- Evolent (Sacramento, CA)
- …when available, within the regulatory timeframe of the request. + Utilizes medical /clinical review guidelines and parameters to assure consistency in the MD ... setting? Join our Utilization Management team as a Field Medical Director, Cardiovascular Specialist and use your expertise in...review process to reflect appropriate utilization and … more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …+ Ensure all omnichannel activities adhere to internal medical , legal, and regulatory standards. + Collaborate with Compliance and Legal to maintain robust ... Experience working within a matrixed environment. + Knowledge of pharmaceutical legal, regulatory , and medical processes. + Strong matrix team-building skills, a… more