- Amgen (Thousand Oaks, CA)
- …scientific strategy and planning and execution for all aspects of clinical drug development across Amgen's clinical programs. This Executive Director within Clinical ... Development will be involved with the full scope of the rare disease clinical drug development activities from the design and execution of Phase 2 through Phase 4… more
- Stanford University (Stanford, CA)
- …aspects of one or more small research studies. Studies may include drug / device trials, longitudinal natural history studies, and other PI-initiated projects dealing ... studies, and work under the close direction of the manager (CRM), regulatory specialist and principal investigator(s). The CRCII will support industry, federal and… more
- GE Aerospace (San Ramon, CA)
- …the Finance teams and the organization on statutory accounting, filings and regulatory requirements. Assist financial reporting teams as required to ensure all ... filings are completed timely, efficiently and in compliance with state regulatory requirements. + Developing expertise within function. Growing reputation within the… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …(CAPA), Deviations, and Change Control** , ensuring compliance with global regulatory requirements and internal standards. The successful candidate will lead ... alignment with corporate quality objectives + Cross-functional Leadership:Collaborate with Regulatory Affairs, Technical Operations, Manufacturing, and Supply Chain to… more
- AbbVie (Irvine, CA)
- …author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: + Based on strong medical and scientific experience, ... knowledge of compliance and regulatory requirements, Allergan Aesthetics customers, markets, business operations and emerging issues , manage the design and… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other program documents. *May oversee… more
- Stanford University (Stanford, CA)
- …overall implementation of assigned research protocols, ensuring efficiency and regulatory compliance. Key responsibilities will include recruiting and screening ... Case Report Forms, as well as reporting serious adverse events and managing drug accountability, supplies, and equipment. The CV Med Clinical Research Team (CCRT) is… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other program documents. *May oversee… more
- Black & Veatch (San Marcos, CA)
- …as wellfield development, aging wellfield infrastructure, rehabilitation, operations, regulatory compliance, aquifer storage and recovery systems, injection wells, ... intrusion, brackish groundwater development and treatment, brine management, and evolving regulatory frameworks. This role is ideal for someone who thrives in… more
- Stanford University (Stanford, CA)
- …of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and ... assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will… more