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This position will be responsible for supporting and contributing to the development and execution of robust health economics, outcomes research, epidemiology and real-world evidence plans that are aligned with brand strategies, medical affairs strategies, clinical development plans, support product value propositions, and optimize market access.
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A minimum of 8 years in clinical practice with outcomes research experience, or 5 years experience in drug development or related discipline in the field of biotechnology or real-world evidence.
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This position reports to Head of Biostatistics and Data Management (BDM) within Research and Development (R&D) Department at SPARC. Main responsibilities will include effective leadership, planning and oversight within the Clinical Data Management (CDM) function as well as facilitating collaboration across all R&D functions to ensure rigorous collection and analysis of data.
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Participate in professional development opportunities to enhance teaching effectiveness, stay current with STEM education trends and research, and contribute to the school's ongoing improvement efforts.
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Prospect Research and analyze the business environment for industry trends and competitor services/ offerings. The business Development Officer will be responsible for leading complex sales opportunities, with a focus on revenue growth across all Pershing X products and services.
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Interface broadly with key functions including discovery sciences, preclinical development groups, toxicology, clinical operations, drug metabolism, regulatory affairs, and late-stage clinical research.
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We help clients with new skilling, talent strategy, leadership development, employee experience, transformational change management and beyond. Collect, prepare, distribute various tissues for in vitro analysis and biomarker evaluation (e.g. WB, ELISA, histology.
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10 years combined experience in academic/clinical and/or industry oncology clinical research and drug development, including experience as lead medical monitor or principal investigator of an oncology trial.
$411,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Along with research, development and innovation that explores new frontiers in learning and measurement our educational measurement solutions and research contribute to the development of new methods and tools, inform important dialogue with education policymakers, and shed light on critical issues and potential solutions - all with the aim of creating a world where all learners can improve their lives through education.
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Perform contract and subcontract administration support tasks by engaging with internal and external stakeholders, including contract closeout activities, coordinating contract review and execution, research, and drafting correspondence such as 75%/85% limitation of funding letters, key personnel change request letters, labor category change requests and other required notices.
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The Position The Director - Epidemiology leads the development and execution of observational research studies completed in line with the needs identified during the annual Evidence Generation Plan (EGP) process at NNI, acting as Primary Investigator (PI) on the execution of Real World Evidence (RWE) studies which utilize data sources within the Novo Nordisk data platform and acting as PI / providing support as a study team member for additional RWE studies performed with external data sources.
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Familiarity with common consumer marketing research tools and techniques such as Nielsen or IRI data. Assist in the development of the brand’s integrated marketing plan. Familiarity with common consumer marketing research tools and techniques such as Nielsen or IRI data.
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Execute the integrated marketing plan, ensuring consistency with brand strategy and brand communication plan. 2-4 years in Marketing (CPG, OTC, Cosmetics). Be accountable for the execution of specific brand activities (e.g. media plan, consumer and trade promotion activities, special packs, sampling, PR programs, event marketing, direct marketing, etc.
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The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Minimum of - years of experience in data analysis, statistical modeling, and data visualization, preferably within the biopharma or healthcare industry.
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Experience with Medical Affairs activities including but not limited to, KOL engagement, clinical research, drug development, commercial planning and medical strategy. The Head of US Medical - Endocrine Medical Affairs will report to the US General Manager with primary responsibility to lead the US Medical Directors and ensure the compliant execution of all medical programs and functions associated with the late-stage development and medical aspects of commercialization of endocrine assets at Ascendis Pharma.
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research development jobs in Lawrence, NJ
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