- GRAIL (Menlo Park, CA)
- …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... and accurate. + Perform study startup activities such as study protocol review , Clinical Data Management Plan (CDMP) development, and Electronic Data Capture (EDC)… more
- Catalent Pharma Solutions (San Diego, CA)
- …annually. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical ... and common standard lab practices in order to assess the quality of pharmaceutical products under cGMPs (as applicable) and limited supervision. This position gives… more
- Catalent Pharma Solutions (San Diego, CA)
- …annually. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical ... with clients with minimal assistance from the department head + Generation and review of manufacturing batch records, manage Catalent San Diego Master Batch Record… more
- Centene Corporation (Sacramento, CA)
- …and clinical monitoring activities. + Participate in decisions regarding the pharmaceutical services within assigned scope including: + Assessing the patient's ... general pharmaceutical needs + Planning for the pharmaceutical ...+ Assess responses to therapy, patient compliance, and ongoing review of drug regimens; report and manage adverse events… 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
- 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 ... and Collaborative Research program. + Provide detailed and compliant medical review and approval of external resources, communications, and publications - ensuring… more
- Bristol Myers Squibb (San Diego, CA)
- …to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents + Conduct investigator ... and nonclinical studies into clinical development opportunities + Oversee Data Review and Independent Data Monitoring Committees + Conduct clinical trials using… more
- Boehringer Ingelheim (Fremont, CA)
- …is the business process owner for BioMES business processes such as templates, review , etc. As an employee of Boehringer Ingelheim, you will actively contribute to ... for BioMES business processes such as batch record templates, review processes, content requirements for batch records, etc. +...(4) to six (6) years' experience in a GMP Pharmaceutical manufacturing environment. + In lieu of a Bachelor's… more
- Taiho Oncology (Pleasanton, CA)
- …the execution of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting of clinical trials. Performance Objectives: + ... as required. Education/Certification Requirements: + Masters level degree in pharmaceutical or related medical science is preferred. Bachelor's level candidates… 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 ... timely execution of contracted studies + Create study metric trackers + Review abstracts and/or manuscripts that result from supported studies + Support closure… more