- BeOne Medicines (San Mateo, CA)
- …play a critical role in safeguarding the integrity, safety, and quality of clinical research processes and data. This position requires: + Extensive knowledge ... General Description: This position within R&D Quality is a senior Auditor role (as Lead or Co-auditor) who is responsible for independently overseeing and conducting… more
- BeOne Medicines (Emeryville, CA)
- …Collaboration** + Serve as the key stewardship liaison for functional partners ( Clinical Ops, Safety, Regulatory , Portfolio, Research ). + Collaborate ... As Senior Manager, Data Steward, you will lead stewardship...domains, ensuring data quality, compliance, and usability across the research and development value chain. Leveraging your subject matter… more
- Eisai, Inc (New York, NY)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... or channel-specific. Essential Functions Present the economic value proposition and clinical benefits of Eisai product portfolio to assigned regional payer account… more
- BeOne Medicines (San Mateo, CA)
- …scientific subject, or equivalent related experience** **Experience:** **Minimum 7+ years' clinical research and development programming experience using SAS** ... **Position Summary:** **The Senior Manager, Statistical Programming is responsible for the...programming.** **Oversee the work of staff in support of clinical trials, ad-hoc analysis requests, data validation, etc. in… more
- BeOne Medicines (Emeryville, CA)
- …: Experience applying **knowledge graphs** and ontology-driven reasoning to drug discovery, clinical data integration, or molecular research is a strong plus. ... We are seeking an accomplished Senior Manager AI Engineering to provide technical leadership...for conveying complex AI concepts to diverse audiences, including research , regulatory teams. + Deep appreciation of… more
- BeOne Medicines (San Mateo, CA)
- …experience in healthcare analytics settings using R or SQL, SAS required; 3+ years' clinical research and development programming experience using R or SQL, SAS ... and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications as needed. + Understand and execute… more
- Merck & Co. (Rahway, NJ)
- …and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal ... strategies for assigned drug-device combination product program(s) for successful clinical introduction(s) and commercial market(s) approval(s).Define design input(s)/ output(s)… more
- Merck & Co. (Rahway, NJ)
- …applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The Principal Scientist is a senior scientific role tasked ... Job DescriptionThe Biologics Analytical Research & Development department of our company ...of release, characterization, and stability assays for testing of clinical trial material and in support of product and… more
- Eisai, Inc (Cincinnati, OH)
- …international regulatory /ethical guidelines relevant to the pharmaceutical industry & clinical trial conduct, and to ensure compliance with these external as ... is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines,… more
- Eisai, Inc (Cincinnati, OH)
- …customer business, disease state, product prescribing information, approved promotional clinical trials, patient access to medication, and regulatory /compliance ... in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of...your profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales… more
