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Remote work schedule available, although hybrid (3 days in-office) work schedules will be considered for candidates in Houston, Austin, Princeton, Salt Lake City, or Pittsburgh. Juris Doctorate, strong academic credentials and at least seven years of experience in a nationally recognized law firm or in house legal department.
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Technically proficient in the following standard chemical procedures and physical measurements (wet chemistry): GC, GCMS, FTIR, HPLC,NMR, pH, acid value, peroxide value, oil content, water content, specific gravity, refractive index, Tg, optical rotation, salt content, solid content, color, ester value and other standard tests.
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Provide primary legal counsel and strategic advice for business units and corporate groups on real estate matters across NRG as well as subject matters expertise in related fields to assist other corporate activities including, development, procurement, M&A, litigation; responsible for implementing NRG's strategic goals; ensuring appropriate risk management as well as compliance with law and NRG's codes of conduct.
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Successful track record of leading through influence and working across complex, global organizational matrix. Ability to create a clear purpose, global vision, strategy and key priorities for competing successfully in the evolving pharmaceutical and health care industry.
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At Genmab, our global data & analytics team develops robust data engineering pipelines by applying industry best practices and ground breaking technology platforms. Senior Manager, Data Engineer, Global Data & Analytics page is loaded.
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At Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
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The Vice President of Global Strategic Regulatory Operations (GRSO) reports directly to the Senior Vice President of Global Regulatory Safety and Biometrics (GRSB) and is a member of the GRSB Leadership Team. As such, this position has accountabilities for the sustained health, growth and continuous improvement of the GRSB organization, inclusive of developing effective partnerships with critical stakeholders across the BMS enterprise.
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Knowledge of Global Drug Development functions (Portfolio and operations, Clinical development, Biometrics & Data Science, Regulatory, Patient Safety) is a plus. As part of the GDD Data & Analytics team the incumbent will gain visibility into business processes by supporting data landscapes for multiple functional areas such as (but not limited to) Global Clinical Development, R&D Portfolio Operations, Global Regulatory Sciences, Global Biometrics and Data Sciences, Worldwide Patient Safety etc.
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We sell the latest AI technologies from Nvidia, Supermicro, Dell, HP, Microsoft, Google, Cisco, Lenovo, Apple, VMWare, Adobe, APC, IBM, Nutanix, EMC, Pure Storage, Samsung, Intel, Eaton, and all the hottest AI and Green Data Center, Virtualization, Energy Conservation, Cloud, Storage, Security, Wireless, SD Wan, Video, Identification, solar, and battery technologies.
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The Drug Safety & Pharmacovigilance (GDS&PV) Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned Genmab products (mainly investigational) throughout their lifecycle.
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This position is under the direct supervision of the Corporate Vice President, Global Operations & Supply Chain. Serves as a key leader within Global Operations (GOPs); Participates in strategic and tactical planning & execution to ensure GOPs objectives are met.
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Serve as the safety expert accountable for the global safety strategy and overall safety profile for assigned Genmab products (investigational) throughout their lifecycle, including leading all major pre- and post-marketing safety related deliverables, including signal, benefit-risk evaluation and risk management activities.
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The individual will support the development and implementation of the Global FPA modules of the future-state planning solution, serving as SME and power user for OneStream ensuring adoption and user readiness.
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Takes a hands-on approach in leading the completion of IND/CTA, NDA/BLA/MAA, and other global submission documents. The Director will be responsible for providing global regulatory leadership in support of the development, registration, and life-cycle management of our innovative gene therapy programs, as well as for the oversight and mentoring of a growing regulatory team.
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As our Account Director for the region, you will work closely with our internal support teams to ensure that churn (customer turnover) is minimized and that customer relationships grow. Zycus is a pioneer in Cognitive Procurement software and has been a trusted partner of choice for large global enterprises for two decades.
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salt job Title: global account Company: Eaton in Princeton, NJ
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