- Merck & Co. (South San Francisco, CA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director… more
- Merck & Co. (South San Francisco, CA)
- …studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Job DescriptionThe Clinical Director ( Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving… more
- Merck (South San Francisco, CA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Senior Director (Sr. Principal Scientist) has...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior … more
- J&J Family of Companies (Irvine, CA)
- … regulatory and quality requirements. + Collaborate closely with R&D, Quality, Regulatory Affairs , Manufacturing, Supply Chain, and Commercial to align on ... at https://www.jnj.com/medtech **We are searching for the best talent for a** Principal R&D Consumables Engineer based in Irvine, CA. **Purpose:** The Principal… more
- Herbalife (Torrance, CA)
- …formulas. ? Collaborate with global cross-functional teams including Quality, Procurement, Regulatory Affairs , Project Management, and Supply Chain. ? Provide ... Principal Scientist, Process & Manufacturing Excellence Category: Research...Herbalife nutritional products, ensuring alignment with business goals and regulatory requirements. ? Apply the Quality by Design (QbD)… more
- Merck (South San Francisco, CA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The **Clinical Director ( Principal Scientist)** has primary responsibility for the strategic planning and directing clinical research activities… more
- Abbott (Pleasanton, CA)
- …information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. + Medical device industry experience. + ... to restore their health and get on with their lives. The Systems Principal Engineer is accountable for delivering entire programs or complex, significant portions of… more
- Bristol Myers Squibb (Brisbane, CA)
- …of key functions (eg, early development, TM, clinical pharmacology, toxicology, regulatory , HEOR, market access, medical affairs ), applying foresight, scientific ... and will supervise and have accountability for the clinical components of regulatory filings. * Will contribute to overall Therapeutic Area disease strategy while… more
- Edwards Lifesciences (Sacramento, CA)
- …Provide medical writing expertise and collaborate with cross functional teams including Regulatory Affairs , Biostatistics, R&D, QA and Marketing on clinical data ... and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and … more
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