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They are accountable, with the Precision Medicine Technical Lead to support BMS product Development Teams (DT) to successfully shape and execute the various translational and diagnostic strategies, projects, and lifecycle plans.
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The Deputy General Counsel, Codman Specialty Surgical will report to the General Counsel, U.S. and will have primary responsibility for handling or managing a variety of general corporate and commercial contracting matters and will provide advisory services to CSS leaders, including the division president as well as sales, marketing, regulatory, quality, clinical and product development leaders.
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This includes but is not limited to responsibility for genomics and gene expression profiling (GEP) biomarker assay technology/ platform selection, evaluation of in-house or vendor choice per assay use requirements, development, optimization, qualification/validation and/or execution of biomarker analysis for BMS translational medicine and clinical programs.
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Our curriculum focuses on the six ages and stages of early childhood development and engages children in hands-on learning activities that encourage them to explore and solve problems at their own rate of development.
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ZS is looking for an experienced team member that brings pharmaceutical drug development and tech transfer knowledge with a focus on digital transformation in this space. Hands on experience with at least one of the functions in CMC development such as Process Chemistry, Process Engineering, Formulation, and Analytical Chemistry.
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As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values and will be responsible for providing statistical expertise/input in the drug development, including clinical development plan and regulatory submission strategy.
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Assist the Director in management, supervision, training, and development of IT audit staff. Responsible for execution of assigned IT SOX testing, IT operational audits, administration of the department audit management system, and development of audit staff.
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A proud U.S. Department of Energy National Laboratory managed by Princeton University, PPPL is a longstanding leader in the science and innovation behind the development of fusion energy — a clean, safe, and virtually limitless energy source.
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A Japan-based company, our goal is to make people smile by delivering breakthroughs where no adequate treatments currently exist, working from drug discovery to product development and commercialization.
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Discuss strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex analysis issues, FDA issues, and general drug development. This is a strategic and critical role in the development of protocols and statistical designs for approval of drug products in different phases of the clinical trials.
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Development and implementation of comprehensive site investigations by participating in scope of work development, field work, and data analysis to characterize contaminants in sediments, soil, air, surface water, and groundwater.
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The responsibilities of the groups include providing bioanalytical leadership on BMS drug development teams via scientific/technical expertise and strategic input; overseeing and/or performing assay development/ validation, and sample analysis; supporting discovery studies for biotherapeutics and regulated and non-regulated bioanalysis for toxicology and clinical studies; and preparing appropriate documentation and/or interacting with health authorities on the BA portion of regulatory filings.
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We are seeking a Senior Civil Engineer with broad expertise in land development and/or site/civil/heavy construction project management to perform investigations and analyses, prepare reports, and provide expert testimony where technical knowledge, skill, experience, training and/or education are needed to help resolve civil litigation and insurance claims.
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The Senior Director of Youth Development will ensure that the Princeton YMCA's programs establish and maintain a level of excellence in areas of quality, creativity and visibility, and support the goals and priorities of the Princeton YMCA. The programs will work to benefit participants, and will provide a positive image of the YMCA within the community, in accordance with the mission and philosophy of the Princeton YMCA.
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Leadership of a cross-functional oncology drug development team with working knowledge across multiple R&D functions (preclinical, clinical, regulatory, CMC) Genmab is seeking an experienced Global Program Leader (GPL) for our antibody product development programs.
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development job Company: Thermo Fisher Scientific in Princeton, Parkville, Maryland
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