- 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 ... + Represent a clinical study or development program on one or more teams or sub teams + Create clinical study or program-related slide decks for internal and external use + Build and maintain opinion leader/investigator networks; organize and present at key… 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... data + Interpret, and present clinical trial data both internally and externally + Represent a clinical… 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... data + Interpret, and present clinical trial data both internally and externally + Represent a clinical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead's products. You ... Phase I studies. + With guidance, may lead contract research organization ( CRO ) and vendor selection and, where applicable, manages all interactions and deliverables… more
- BeOne Medicines (Emeryville, CA)
- …of comparator drugs used in study for countries in region + Manages the trial data collection process for the region, drives data entry and query resolution + ... years of progressive experience in clinical research within biotech, pharma or CRO industry + Proven experience in clinical research including relevant experience as… 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... data . + Interpret, and present clinical trial data both internally and externally. + Represent a clinical… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …highest quality and meet global regulatory reporting timelines. Responsible for data review, compilation and analysis including management of the integrated safety ... of relevant experience in pharmacovigilance, clinical research, or regulatory affairs in a CRO or a pharmaceutical company is usually required. + 2-3 years of… more
- Actalent (San Francisco, CA)
- …Lead and participate in activities ensuring quality, consistency, and integration of study data to meet agreed time, cost, and quality objectives. + Interface with ... + Strong operational and vendor management skills. + Combination of sponsor and CRO experience. Work Environment The role is fully remote, with team members located… more
- Charles River Laboratories (Northridge, CA)
- …* Perform internal and external supplier audits. * Manage the inspection/back room during regulatory or customer audits. * Review validation reports (IQ/OQ/PQ) * ... the management of Quality System Reports (QSRs), including deviations, change control , corrective and preventive actions (CAPA), exceptions, customer complaints, and… 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 ... with inventory accounting in the pharmaceutical industry, a plus * Experience with CRO /CMC accrual software, a plus * Certified Public Accountant (CPA), preferred *… more
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