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The research assistant will be responsible for performing tissue culture and basic molecular and biochemical lab techniques (PCR, immunoprecipitations, western blots) and will have the opportunity to learn early drug development, proteomics, and genomic screening approaches.
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As the Supervisory Associate Director for Real World Evidence Analytics (RWE) (Supervisory Physician) , the incumbent provides strategic vision for the agency’s effort to evaluate and promote the use of RWE to advance drug development and to further evaluate the safety and effectiveness of marketed therapies.
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Successfully perform telepharmacy services to assigned clients including remote order entry, order verification, drug verification, and counseling (when required). Provide leadership, vision, development, and implementation of telepharmacy goals as relayed by the Regional Manager.
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Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.
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Knowledge of CMS claims data, including Medicare, Medicaid, and Marketplace, in the IDR or CCW environment with Fee-for-Service ( FFS ) , Medicare Advantage encounter data, Medicaid data in the Transformed Medicaid Statistical Information System ( T-MSIS ) , or Prescription Drug Event ( PDE ) data.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Lead state of the science and state of the system analysis for various health projects, which can include landscaping of latest scientific research, experimental therapies, industry pipelines, key research players, drug development models, key nonprofit and advocacy stakeholders, etc.
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As a CoStar Technical Manager on the Platform Development team you will play a key role in expanding the data platform that supports all of CoStar Group’s largest brands including Homes.com, CoStar Suite, LoopNet and Apartments.com. You will deeply understand what drives the business for which you are building software.
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During this Fall 2024 internship, the LRA intern will gain exposure to the world of health care policy and have the opportunity to work on various projects related to advancing rare disease research and innovation both with Congress, the FDA and NIH. Anticipated focus areas include reauthorization of the Rare Pediatric Disease Priority Review Voucher program, advancing Patient-Focused Drug Development, and the next Prescription Drug User Fee Act cycle.
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Implement the Tools of the Mind curriculum with the guidance from the Reggio Emilia philosophy to promote children's development and learning. While some jurisdictions, including Maryland, permit the use of marijuana for medical purposes, marijuana continues to be classified as an illegal drug under the federal Controlled Substances Act. As a result, medical marijuana use will not be accepted as a valid explanation for a positive drug test result.
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Technical Skill Set:7+ years of software development experience in one or more of the following programming languages: React, TypeScript, JavaScript, Ruby, Ruby on Rails, and/or Go/Golang. The 340B team supports and advises pharmaceutical manufacturers on navigating the challenges and complexities of the 340B program, a government drug purchasing program.
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Stay abreast of the latest developments in the field of R, statistics, and quantitative sciences in drug development and contribute to scientific advances in the field. In this role, we are looking for individuals with a quantitative science background (statistics, data science, computer science, mathematics, or similar) and passion in drug development to join an R analytic group within global statistical science at Amgen.
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With outpaced growth across the industry and advancements in drug development this is undoubtedly a transformative time for regulators, developers, and patients. Experience working with the US Food and Drug Administration (FDA) or related Department of Health and Human Services (HHS) operating division in the past 12 months.
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The Executive Director, Human Capital Management, oversees the Program Office that directly impacts the human capital management lifecycle, including recruitment and retention, onboarding, performance management, workforce planning, training, benefits, retirement counseling, leader development, talent management, employee engagement, human capital policy, employee and labor relations, diversity and inclusion, safety, workers compensation and emergency management.
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Also includedare campus security policies including those related to missing student notifications, alcohol and drug use, sexual assault, relationshipviolence, and stalking, crime prevention, the reporting of crimes, and fire safety policies and statistics.
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drug development jobs in Washington, DC
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