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Familiarity with product lines including Crestron, Extron, Samsung, BiAmp, Clearone, QSC / Q-SYS, D&B sound system, Shure, Yamaha CL5, Barco (E2), High End Systems, Neat, Poly, Cisco, BrightSign, etc.
ExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Industry Enablement skills: (consulting, design & development, training facilitation skills, presentation, program management, stakeholder management, and whiteboarding). Experience in learning design (e.g. Bloom taxonomy) and measurement (e.g. Kirkpatrick framework), enablement tooling (Learning management, content management, and Articulate/RISE), gamification, and program management across multiple stakeholders (i.e. "master herder of cats.
$150Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Primary duties of the Trash Collector include: - Operating garbage trucks - Collecting and dumping trash receptacles - Following route assignments as directed Waste Management offers an excellent benefits package that includes medical, dental, vision, life, 401(k) savings and more.
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Strong understanding of science and drug development, with specific expertise in nonclinical study design, preclinical CROs, data management systems, nonclinical study procedures, and statistical analysis methods.
$250Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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4+ years of experience in product management leading complex product launches with cross-functional teams, demonstrating exceptional leadership and project management skills.
$120,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The Policy Advocacy Director-State Alliances will engage state and regional-based external stakeholders, including patient and provider advocates and associations on Gilead’s policy priorities –including price setting policies like Prescription Drug Affordability Boards and the Inflation Reduction Act, the 340B Drug Discount Program, as well as policy issues associated with access to screening, treatment, and care pertinent to virology and oncology therapeutic areas.
$201,025 - $260,150 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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5+ years of experience in drug discovery with proven leadership of preclinical development of therapeutic project(s) and clinical candidate selection is a requirement. Experience as a project team lead (PTL) in a drug discovery setting for biologics programs.
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Responsibilities will also include data processing, statistical analysis, and dissemination of results to project teams in support of drug discovery and development programs. The responsibilities of a DMPK Bioanalysis Research Associate contract position are to develop and routinely employ bioanalytical methods for the qualitative analysis of small molecules in plasma, and various biological tissues using liquid chromatography-mass spectrometry in support of drug discovery.
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Works collaboratively with Clinical Operations, Formulation Process Development, Device Development and Clinical Package Engineering, Quality Assurance, Regulatory, Outsourced Manufacturing and Project Management partners to develop optimal supply strategies and ensure on time delivery of clinical supplies to initiate and resupply studies with investigational medicinal product (IMP.
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You’ll collaborate with leaders in Engineering, and Product Management teams to create innovative experiences across Spotnana product offerings, leveraging your passion for brand, craft, and design quality.
$200,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Demonstrates knowledge of global clinical trials and the drug development process, Knowledge of IRT system setup and functionality and proficiency with Excel modeling, Strong collaboration and excellent team skills to be successful in cross-functional and multi-cultural teams.
$74 - $82 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This position has primary responsibilities for setting strategy across the clinical development program, oversight of strategic study design, study start up, CRO and vendor management, clinical data and safety monitoring, analysis and reporting of studies.
$225,000 - $275,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Possess clinical supplies experience/knowledge in forecasting, demand / supply planning, IRT systems, inventory management, clinical labeling and distribution including cold chain, import/export, and reverse logistics.
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Leads end -to-end clinical supply responsibilities including but not limited to protocol interpretation, demand planning, supply planning, distribution, inventory management, label generation and planning and execution of labeling operations at partner contract manufacturing organizations (CMOs.
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You will collaborate closely with cross-functional teams (R&D, clinical, Software Engineering, Process Engineering, Product) to support new assay development and existing assay enhancements, with a strong emphasis on scaling and workflow efficiency.
$200,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
product management drug jobs Title: development director Company: Omeros in Redwood City, CA
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