- Sumitomo Pharma (Sacramento, CA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... on external engagement, MSL/cross functional input and impactful insights, supporting data generation, and data communication, education and awareness… more
- Sumitomo Pharma (Sacramento, CA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... transactional IP support, with an emphasis on patent litigation in the pharmaceutical /biotech industry. As a partner and key business strategist, this individual… more
- Sutter Health (Sunnyvale, CA)
- …PAMF-Palo Alto Medical Foundation CAD **Position Overview:** Delivers pharmaceutical care through the provision of patient-centered clinical service, ... collaborative practice agreement or an approved protocol. + Completes medication regimen review from a clinical, safety and cost perspective to identify duplicate… more
- ThermoFisher Scientific (San Diego, CA)
- …specifications, method validation and transfer. + Previous stability management and analytical data review experience is highly desired. + Experience in managing ... employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. **Key… more
- GRAIL (Menlo Park, CA)
- …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 ... United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com… more
- Stantec (Roseville, CA)
- …compliance specialists delivering EHS and sustainability solutions to commercial, pharmaceutical , food and beverage, manufacturing, mining, oil and gas, power, ... Contractor Safety Program - Training plan recommendations and requirements - Safety Program review and recommended updates - Safety Culture assessment review and… more
- Actalent (Newbury Park, CA)
- …in a dynamic, fast-paced environment. Key Responsibilities + Conduct QC review of analytical data for starting materials, intermediates/in-process controls, ... spectroscopy. + Strong attention to detail with proven ability to interpret and review analytical data . + Proficiency in Microsoft Office, especially Excel. +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Medical Affairs team. This role is responsible for leading the Phase 4 RC review process and portfolio management of Gilead and Externally Sponsored research in HIV ... of contracted studies + Create study metric trackers + Review abstracts and/or manuscripts that result from supported studies...to ensure inclusion of ISR and CO studies in data generation plans + Prepare presentation materials related to… more
- Cardinal Health (Sacramento, CA)
- …+ Meticulous attention to detail + Ability to manage multiple large and small pharmaceutical data sets + Ability to switch between projects with competing ... regulatory affairs and product development consulting services to enable pharmaceutical , medical and biotechnology companies to obtain regulatory approvals. More… more
- AbbVie (Irvine, CA)
- …across assets with similar MOA + Leads and guide the safety physicians on data review (clinical and beyond) and interpretations across assets with similar MOA ... to effectively conduct safety surveillance + Responsible for safety surveillance for pharmaceutical / biological / drug -device combined products + Lead and set… more