- Gilead Sciences, Inc. (Foster City, CA)
- …and management of content license agreements + Partnering with Legal on the review and approval of license agreements + Managing employees or contingent workers ... MD and 6 years' Experience **Preferred Qualifications:** + Experience in pharmaceutical , healthcare, or information management industry preferred + Advanced level… more
- Gilead Sciences, Inc. (Foster City, CA)
- …lymphoma, leukemia, and multiple myeloma + Work independently to prioritize, execute, review , and edit key tactics consisting of congress abstracts and presentations ... Advanced degree (Pharm D, MD, PhD) and 2+ years of biotech/ pharmaceutical industry or medical communications agency experience with focus on scientific/medical… more
- BeOne Medicines (San Mateo, CA)
- …during product lifecycle for the assigned project. + Provide CMC regulatory review for clinical protocols and investigator brochures, etc. for the assigned project. ... is a plus. **Qualifications:** + 8+ years of related pharmaceutical or biopharmaceutical industry regulatory CMC experience. + EducationRequired:BA/BSDegreeinscientificdisciplines,MS/PhDpreferred.… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …and management of third-party vendors in support of business relationship. + Review proposed publications, press releases, and external disclosures. + Prepare clear, ... industry and/or law firm experience providing legal counsel relating to devices, pharmaceutical , or therapeutic products. + A Bachelor or advance degree in… more
- Teledyne (Milpitas, CA)
- …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an ... subsystems, to document measured performance and compare to design goals, and to review and guide PCB layout to ensure analog circuitry can perform as designed.… more
- Gilead Sciences, Inc. (Foster City, CA)
- …expert witness work, and preparation for key hearings and trial. Review correspondence, arguments, memos, and briefs in support of litigation, investigations ... years of relevant and extensive litigation and investigation experience, preferably pharmaceutical , medical device, or life sciences industry experience. + Extensive… more
- Cedars-Sinai (Los Angeles, CA)
- …subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research ... Works closely with investigators and regulatory staff or directly with Institutional Review Board (IRB) to submit adverse events, serious adverse events, protocol… more
- BeOne Medicines (Emeryville, CA)
- …and documents. + Designs and conducts quality issue trending, analysis and review activities to proactively identify broader issues and/or patterns within GCO ... + Bachelor's Degree with minimum of 10 years of experience in pharmaceutical or biotechnology drug development, preferably in a relevant field such as… more
- Teledyne (Thousand Oaks, CA)
- …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an ... layout, setup, operation, and tool adjustments of various types of equipment. + Review and verify dimensions and tolerances in drawings to determine best setup and… more
- Abbott (Santa Clara, CA)
- …preclinical and clinical documentation for submission filing. + Compile, prepare, review and submit regulatory submissions to authorities. + Monitor impact of ... changing regulations on submission strategies. + Monitor applications under regulatory review . + Monitor and submit applicable reports to regulatory authorities. +… more