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The GLP - IPO , based at UMD , serves as a catalyst to achieve the mission of this international network to enable research for sustainable development of land systems via four main objectives: 1) Setting agendas and facilitating synthesis in land system science; 2) Enabling the production of cutting-edge land system science worldwide; 3) Informing science-based policy on land; and 4) Building capacity of the Land System Science ( LSS ) community to deliver inclusive, solutions-oriented science.
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Understanding of scientific principles and regulatory/quality systems relevant to drug development. Advanced scientific degree (MSc, PhD, or PharmD) preferred; Join Takeda as an Associate Director, Global Labeling Lead where you will be responsible for the development, maintenance, and implementation of Company Core Data Sheets (CCDS) in line with international standards and guidelines.
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This is to ensure the distribution of clinical and scientific information regarding in-development or commercialized Regeneron products in a timely, ethical and customer-focused manner. Ability to communicate and disseminate scientific and clinical data in response to unsolicited requests for information as appropriate per medical field policy, using oral presentations, written communications, scientific literature or other approved materials and tools.
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BlackSky is looking for a talented and creative Staff Machine Learning Quality Engineer to support the development, operation, and capability evolution of Spectra AI, BlackSky’s cutting edge AI/ML Platform.
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A bachelor's degree in a relevant field is required as a strong scientific foundation (e.g. molecular biology, engineering, biochemistry, pharmacology) is required for the position. Our client is a privately-owned contract development and manufacturing organization (CDMO) focused on helping clients from pre-clinical to development and commercialization of biologics, medical devices, and combination drugs.
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The community of Banneker Fellows will receive funding for cohort building and professional development activities, including enrollment in the National Center for Faculty Development and Diversity Faculty Success Program, proposal writing training, and seed grants.
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Ability to engineer systems with integrated software and hardware solutions, and sensory control loop development. Bachelor of Science (BS) degree from an accredited college or university in an engineering, scientific, or technical discipline.
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Competency of methodology in development and review of scientific and essential clinical trial / regulatory document. Functional management of Head of Clinical development US and Head of Clinical Development EU and their teams comprised of Clinical Scientists / Clinical Associates / Scientific Experts (PhD) and/or Medical Advisors (MD.
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Member of Organon’s Research & Development Review Committee (RDRC) to ensure scientific and medical soundness of development programs, including preclinical, clinical, and registration enabling medical affairs study protocols, stage-gate transitions and mitigations for issues encountered in development and execution of such programs within agreed upon timelines and budget.
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Provide general and directed IP counsel and education to Inari scientists and management while operationally supporting Inari’s corporate and business development efforts with regard to IP due diligence, competitive intelligence, IP in-licensing.
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Development/support, scientific affairs, operations, or related area. As a manager, the function of a Manager Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation.
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As a Senior Director you will be responsible for leading HEOR-Epidemiology activities to inform, support, and strengthen global development and commercialization activities for our products in the oncology therapeutic area.
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Translational Medicine Hematology at BMS has a long-standing history of scientific rigor as evidenced by our peer-reviewed publications, delivery of drug approvals including Revlimid, Pomalyst, Idhifa, Inrebic, Onureg and Reblozyl, strong academic collaborations and talent development.
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Strong scientific background, bonus points if in medicinal or computational chemistry. 10+ years in biopharma business development, with hands on deal experience. We are looking for a Business Development team member to join our team and help us grow our core business, craft new deal structures, and develop GTM strategies for our offerings.
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The Associate Data Scientist works with the data science team to facilitate and manage clinical data collection for algorithm development, for clinical studies related to FDA submission, and for research and scientific communications purposes.
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