- General Atomics (Poway, CA)
- …Such methods should be based on standards and on rigorous statistical analysis , ideally involving UQ (uncertainty quantification) methods. + Help develop tools for ... **Job Qualifications:** + Typically requires a bachelors degree, masters degree or PhD in engineering or a related technical discipline from an accredited… more
- Gilead Sciences, Inc. (Foster City, CA)
- …staff and contribute to preparation of research reports, manuscripts, and regulatory document filings **Basic Qualifications:** 6+ Years relevant industry experience ... OR 4+ Years relevant industry experience with MS; OR 0+ Years with PhD ; PhD plus postdoctoral training preferred **Preferred Qualifications:** + Experience… more
- General Atomics (San Diego, CA)
- …to resolving unusual or complex engineering problems. The role includes the analysis , investigation, and resolution of embedded software and control system problems ... and serial emulators to obtains test data and perform analysis . + Applies technical knowledge to train others in...+ Typically requires a bachelors degree, masters degree or PhD in engineering or a related technical discipline from… more
- Bristol Myers Squibb (San Diego, CA)
- …Diseases. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... collaborators to develop translational analysis plans and timelines, communicate analysis results....scientific, technical or medical journals. + **Qualifications** : + PhD degree in a neuroscience-related field + Minimum of… more
- University of Southern California (Los Angeles, CA)
- …and/or behavioral interventions, the development of study protocols and regulatory materials, and the development of human laboratory protocols involving ... use disorders. The fellow will also have opportunities for leadership roles in data analysis and manuscript writing, and will act in a leadership capacity for junior… 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. ... for key deliverables. *Primary responsibility for and ownership of design, analysis , interpretation and reporting of scientific content of protocols, Investigator… more
- Pfizer (South San Francisco, CA)
- …clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + Provide leadership to ... with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists. Meet regularly with the Pfizer Oncology group… more
- Cedars-Sinai (Beverly Hills, CA)
- …students on selecting appropriate research methodologies, data collection techniques, analysis tools, and interpretation of findings, ensuring projects are executed ... keep on track with new regulations/compliance policies in clinical and regulatory sciences. **Qualifications** **This role follows a hybrid work schedule; however,… more
- AbbVie (South San Francisco, CA)
- …and timeline improvement. Set up automation of wet lab and data analysis workflows. + Design and perform experiments for engineering gene knock-in/-out/-down in ... lab notebook. + Author detailed technical reports that support regulatory filings at all stages from IND to BLA....Master's Degree with 8 years of relevant experience, OR PhD with no experience. + Proficiency with molecular biology… more