- Astellas Pharma (South San Francisco, CA)
- …as a project toxicologist + Lead discussions on the design, execution, data analysis and interpretation of toxicology studies. + Conduct microscopic examination of ... studies. + Conduct peer reviews of studies performed at CROs. + Report pathology data in accordance with GLPs. + Communicate study results and their relevance to… more
- BeOne Medicines (San Mateo, CA)
- …Area Global Medical Affairs Plan. + Develop and execute on a data generation strategy outside of the clinical development program, including investigator -initiated ... area advisory meetings. + Interpret, and present clinical trial data both internally and externally. + Partner with the...of, author, update, and/or review. + Train BeOne colleagues, CRO staff, and study site staff on the therapeutic… more
- BeOne Medicines (Emeryville, CA)
- …Health Authorities, and CRO 's + Review, query, and analyze clinical trial data + Interpret, and present clinical trial data both internally and externally ... and report on goals and objectives + Support budget planning and management + Be accountable for compliant business practices **Required Education:** + Advanced… more
- BeOne Medicines (San Mateo, CA)
- …scientific expertise for selection of investigator and vendors + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... and CROs + Review, query, and analyze clinical trial data + Interpret, and present clinical trial data...on goals and objectives + Support budget planning and management + Be accountable for compliant business practices **Education… more
- BeOne Medicines (San Mateo, CA)
- …scientific expertise for selection of investigator and vendors + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... and CROs + Review, query, and analyze clinical trial data + Interpret, and present clinical trial data...on goals and objectives. + Support budget planning and management . + Be accountable for compliant business practices. **Required… more
- BeOne Medicines (San Mateo, CA)
- …scientific expertise for selection of investigator and vendors. + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... and CROs. + Review, query, and analyze clinical trial data . + Interpret, and present clinical trial data...on goals and objectives. + Support budget planning and management . + Be accountable for compliant business practices. **Required… more
- Charles River Laboratories (Northridge, CA)
- …such as Terumo Optia or Trima, which includes set-up, run, quality control , troubleshooting, and routine maintenance with RN oversite. * Performs white blood ... and Registered Nurse on Bone Marrow collection procedures. * Conduct quality control of collection equipment. Bring problems and irregularities to the attention of… more
- Actalent (San Francisco, CA)
- …managing clinical trials from the sponsor perspective. + Strong operational and vendor management skills. + Combination of sponsor and CRO experience. Work ... + Evaluate regulatory packages and manage documents within the Clinical Trial Management System (CTMS). + Supervise study start-up activities and ensure timelines… more
- Vera Therapeutics (Brisbane, CA)
- …understanding of general ledger structure and ensure integrity and accuracy of financial data * Assist with SOX 404 efforts in documenting and performing the key ... system processes, internal controls, GAAP and SOX regulations * Strong project management skills with the ability to anticipate events, prioritize assignments, deal… more
- Charles River Laboratories (Northridge, CA)
- …collection of plateletpheresis, leukapheresis, and whole blood. Partner with other donor room staff to ensure a smooth operation and efficient production of blood ... + Automated plateletpheresis and leukapheresis including set-up, run, quality control , troubleshooting and routine maintenance. + White blood cell collections… more