• Merck & Co. (North Wales, PA)
    …Alliances b) Data Mastering, Data Governance including but not limited to Data Marketplace, Data Quality , Data Risk Management c) Value ... quality value delivery across all aspects of the data value chain including but not limited to a)...Operate with Integrity and ensure adherence with organization policies, quality assurance and data protection processes.Conduct innovation… more
    HireLifeScience (09/06/24)
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  • Merck & Co. (Rahway, NJ)
    …animal species. About the Position The Animal Health IT Customer Master Data Management (MDM) Product Owner collaborates with stakeholders across all levels of ... organization, from senior management to tactical execution- to understand customer master data management needs. With an increased focus on Commercial, Sales, and… more
    HireLifeScience (09/07/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Summary Director , Global Medical Affairs Oncology Publications works with Cross Functional Team ... research organizations, and study investigatorsManage vendor budget and activitiesOversee the quality and timeline of vendor workCollaborate with study medical lead… more
    HireLifeScience (09/11/24)
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  • Eisai, Inc (Nutley, NJ)
    …and make a difference. If this is your profile, we want to hear from you. Director , Global RWE & Data Science sought by a pharmaceutical company in Nutley, ... NJ. Assess real-world data gaps and lead evidence generation process for the...that address issues such as payer challenges, impairments in quality of life and patient well-being, and gaps in… more
    HireLifeScience (08/27/24)
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  • Merck & Co. (South San Francisco, CA)
    …and innovation as the head of a group responsible for delivering high quality characterization data to advance discovery programs from the high-throughput ... are seeking an exceptional and experienced leader in the role of Director of Biologics Analytical Characterization and Developability in the Protein Sciences… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …investigators is expected. The CS Group Lead will also ensure the writing of high- quality clinical trial protocols, review of clinical data and Clinical Study ... multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical Science...of ICF, DM charter, response assessment charter, etc), clinical data review excellence with a focus on patient safety… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for producing scientifically ... accurate, high- quality clinical regulatory documents while adhering to regulatory guidelines....strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Associate Director of ERP Applications is responsible for overseeing and enhancing designated ... from all Daiichi Sankyo regions in scope.- Responsible for developing high quality solutions based on Functional Design documents. Perform system customization and… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, ... and executing post-approval Regulatory CMC strategies, reviewing CMC information and data , authoring CMC submissions, and interacting with Health Authorities to meet… more
    HireLifeScience (09/11/24)
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  • Merck & Co. (Rahway, NJ)
    …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
    HireLifeScience (09/08/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …review teams as well as with business partners to achieve high quality and accurate labeling in support of business objectives.ResponsibilitiesPreparation of new and ... updated Core Data Sheets, EU and US Documentation: As the project...Global Labeling Operations and Compliance leads to product high quality labeling documentation.Establishes Process Best Practices: Serve as a… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …related to study, project and submission. Manage CRO to ensure high quality compound and multi-compound level deliverables. Lead the development of global ... Statistical Programming Management: Coordinates outsourced statistical programming of analysis data sets and tables, listings, and figures (TLFs) needed for… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …direction to Biostats Data Mgmt & Data Ops for EDC, edit checks, data quality listings, SAP, Data Mgmt plan; Reviews patient population and protocol ... to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Phase 2 studies: Provides the strategic direction to BD&O for EDC, edit checks, data quality listings, SAP, DM plan, Reviews patient population and protocol ... to ensure appropriate biomarker, PK / PD measurements, Reviews emerging clinical data regularly, Leads dose-escalation meetings, Performs quality assessment with… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Phase 2 studies: Provides the strategic direction to BD&O for EDC, edit checks, data quality listings, SAP, DM plan, Reviews patient population and protocol ... to ensure appropriate biomarker, PK / PD measurements, Reviews emerging clinical data regularly, Leads dose-escalation meetings, Performs quality assessment with… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance ... complies with all applicable regulations and guidelines and with Company Core Data Sheets and manages deviations. This position interacts across the RA function… more
    HireLifeScience (09/11/24)
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  • Insmed Incorporated (San Diego, CA)
    …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , Quality Assurance - Analytical,GMP has responsibility for the ... approval of GMP analytical records. Will also provide QA support for GTx Quality Control laboratories. This position is onsite/hybrid and based in San Diego,… more
    HireLifeScience (08/22/24)
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  • Merck & Co. (North Wales, PA)
    …at the forefront of digital transformation in the biopharmaceutical industry. As a Director of Content Management, you will play a pivotal role in simplifying our ... Quality Management System (QMS) technology stack and enhancing user...Management (KM) tools like Kneat. Preferred Experience: Experience with data science, AI implementation, data engineering, or… more
    HireLifeScience (09/08/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Valuation NPV Modeling Financial Support: - Provide independent and high- quality financial support to all BDL transactions including In-Licensing, Out-licensing, ... valuation model, including sourcing and validation of key assumptions and data from global cross-functional teams (Marketing, RD, Finance, Supply Chain, etc).… more
    HireLifeScience (09/11/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …statistical activities; collaborates closely with data manager to ensure high quality data .Drug Development Strategy: Provides input to multiple aspects of ... the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight: Review CRO/vendor proposal and budget.… more
    HireLifeScience (09/11/24)
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