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Your duties will include preparing solutions based on stoichiometric calculation, synthesis functionalized magnetic nanoparticles, purification the resultant magnetic nanoparticles, characterization the composition and the properties of the made materials, examination the performance on phosphorus removal, design, review, conduct the experiment, report and analyze the data to PI.
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The Medical Director reports directly to the Executive Director, Medical & Scientific Affairs. Education: OD, MD (Ophthalmology), PhD (Eye Sciences), or PharmD degree in scientific/biological/clinical discipline.
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Bringing our expertise to new markets, we invest in high-technology materials, 3D printing and hydrogen, to serve a wide a variety of industries—from aerospace to biotech. B.S. degree in scientific field and 0-5 years’ experience in process engineering or quality control manufacturing environment or equivalent experience in process engineering or quality manufacturing environment.
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This role requires expertise in crafting effective messaging, managing communication campaigns, and engaging with diverse stakeholders to promote public health initiatives and scientific research.
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Partner with the asset lead, GPTs, and study teams to establish and oversee Diversity Plans (DP) and patient voice on the indication and study levels, taking into consideration the epidemiology of the disease -Review applicable study specific clinical trial materials to ensure cultural sensitivity and health literacy guidelines are followed.
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Provide graphic design and editing capabilities related to digital channels, with the ability to create and edit graphics and photos using Adobe Photoshop, Adobe Fireworks, and other design-related applications including, but not limited to, webpages and website graphics, fact sheets, templates for information dissemination, infographics, social media graphics, animated videos, flow charts, logos, brochures, training materials, forms flyers and presentations.
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Leverage expert knowledge across CDC's IMS to coordinate rapid clearance of response-related documents, which include scientific guidance and manuscripts, communication products, and press materials.
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Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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Tanaq Support Services (TSS) delivers professional, scientific, and technical services and information technology (IT) solutions to federal agencies in health, technology, and other government services.
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Translation of scientific data into policy- and consumer-focused materials, such as fact sheets, training materials, publications, web content, and program stories. ORISE Information: This program, administered by ORAU through its contract with the U.S. Department of Energy (DOE) to manage the Oak Ridge Institute for Science and Education (ORISE), was established through an interagency agreement between DOE and CDC. Participants do not become employees of CDC, DOE or the program administrator, and there are no employment-related benefits.
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ASRT, Inc. provides scientific, information management, management consulting, bioinformatics, and administrative program support to the Centers for Disease Control and Prevention (CDC) and other Federal and private sector clients.
$68,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Strong technical writer and editor familiar with science/technology/innovation writing, such as reports on scientific findings and articles for internal and external audiences. Draft and edit a wide range of content to include technical and scientific content to writing short and catchy promotional content, well as collaborate with creative members to guide the development of imagery to accompany the content.
$143,706 a yearFull-timeRemoteExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Advise patent litigation teams based on your technical and scientific area of expertise. You have an advance degree in materials science, chemistry chemical engineering, or a closely related field.
$185,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Must be willing to travel up to 20% of the time for client work within the US. Requirements: College graduate in scientific, medical, clinical discipline or related experience; or minimum of 7 years’ experience in GCP regulated industry if not a college graduate Minimum of 5 years’ experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.
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scientific materials jobs in Atlanta, GA
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