- Gilead Sciences, Inc. (Foster City, CA)
- …possible, together. **Job Description** **Key Responsibilities** Reporting to the Executive Director , Head GHEOR, this role will: + With oversight and guidance ... from Senior Director GHEOR CoE, identify and evaluate topics of key...existing methods and deliverables. + Disseminate HEOR data and study results through publications and integration into approved field… more
- Merck (South San Francisco, CA)
- …Company's South San Francisco site is seeking a passionate and talented Associate Principal Scientist with experience in bioinformatics and statistics to solve ... of fundamental and advanced statistical techniques for non-clinical and clinical studies through publications or patents + Strong command of Python and… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …Participate in study concept, protocol and SAP development for Real World Studies and ensure appropriateness of study design, sample size and statistical ... statistical expertise for analysis of clinical trials data beyond the study endpoints, including secondary, exploratory, subgroup analyses. The overall purpose is… more
- BeOne Medicines (Emeryville, CA)
- … study or program level. **Essential Functions of the job:** + Manages the clinical studies at study and program level as the sourcing lead. + Engages the ... metrics, and vendor oversight/governance. This position will also be responsible for clinical study budget estimation and budget management during the study life… more
- BeOne Medicines (Emeryville, CA)
- **_General Description:_** Work with cross-functional study /project teams supporting hematology studies and interact with Clinical, Regulatory, Statistical ... developing and implementing the statistical analysis plan (SAP) for the clinical study report (CSR) and other health authority submission documents. Provides content… more
- United Therapeutics (Sacramento, CA)
- …Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic or pharma regulatory experience with a Master's ... sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or pharma regulatory...sciences, quality, regulatory affairs or a related area of study + 8+ years of project or people management… more
- Gilead Sciences, Inc. (Foster City, CA)
- …improve CDS quality practices and methods + Work closely with Gilead CDS study team to provide expert advice on compliance issues and risk mitigation actions ... + Collaborate with the audit, inspection and CAPA management team within Gilead R&D Quality on internal audits, regulatory agency inspections, risk assessment, deviations and CAPA activities + Liaison and coordinate with business experts and stakeholders to… more
- GRAIL (Menlo Park, CA)
- …we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to overcome one ... of medicine's greatest challenges. GRAIL is headquartered in Menlo Park, California, with locations in Washington, DC, North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies.… more
- San Jose State University (San Jose, CA)
- …Office, Accounting, Payroll, Service-Learning, and University Personnel + Collaborate with Associate Director for Career Education and career counselors to ... Assistant Director for Career Experiences and Events Apply now...+ Four (4) years of administrative work experience involving study , analysis, and/or evaluation leading to the development or… more
- Gilead Sciences, Inc. (Foster City, CA)
- …that will improve the lives of patients with life-threatening illnesses worldwide. The ** Associate Director , Oncology Market Research IID&D** will assume a key ... aligned and coordinated efforts. + Manages Oncology patient market research studies , including project objective, design, vendor selection and oversight, monitoring… more