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A minimum of a Bachelor’s degree, preferably in Learning and Development, Communications, Education/Adult Education, Psychology, User Interface/UserExperience (UI/UX), or another relevant field is required.
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Global Market Access is the link between research and development and commercial operations. Are you driven to learn about market access, product development and evidence generation to demonstrate the value of our pharmaceutical products to key stakeholders.
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Job Title: Specialist 3 - Training and Development. In this role, you will manage the Innovation and R&D learning content portfolio and design and deliver holistic learning solutions, combining education, experiences, and exposure to support specialized and targeted employee development at scale.
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The YMCA is one of the nation's leading nonprofit organizations dedicated to strengthening communities through youth development, healthy living and social responsibility. With Director of Youth Development, support parent/family communication and follow-up.
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Ashland has an exciting opportunity for a Scientist/Staff Scientist to join our research and development (R&D) group for medical device related products in the Diagnostic Film Group at our Bridgewater, NJ location.
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River Crossing YMCA is a charitable, nonprofit organization committed to strengthening our communities through membership and programs that foster youth development, healthy living, and social responsibility for all.
$20 an hourPart-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Enable security(authentication/authorization) for Mobile App accessing enterprise API. Design and development of Flutter mobile apps/web. Work in agile development methodologies and delivering work assignment on time following 2 weeks sprint cadence.
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Leads strategic consultation, and guidance to the PV scientists on decisions that have significant drug safety implications, including safety signal detection activities of monitoring, evaluation, interpretation and appropriate management and communication of safety information for Insmed’s portfolio of products in development.
$339,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This is a multidisciplinary role & this individual will need the ability to interface with all levels of the organization, including Manufacturing, MS&T, Quality Assurance, QC, Process/Analytical Development, Supply Chain, Training, Engineering/Facilities, HS&E, and Finance.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Pharmacokinetics, Dynamics, and Metabolism (PKDM) department at Sanofi contributes to the safe and effective therapeutic treatment of each patient by applying appropriate pharmacokinetic (PK) and pharmacodynamic (PD) principles to drug development and accelerating the process, where possible.
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Familiarity with and exposure to drug discovery and clinical development processes with one or more of the following therapeutic areas: oncology, immunology, cardiovascular, neuroscience, pulmonary hypertension, or infectious disease.
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The Advanced Practice Nurse will be an integral part of the health care team, working with physicians, nurses and nursing or medical assistants to provide comprehensive high-quality ambulatory care, as appropriate to the ages of the patients growth and development through the life cycle factors.
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Monitor assay development, assay validation and sample analysis processes, ensure timely delivery of quality results in compliance with regulatory guidance. Act as the project manager to support the externalization and operationalization of clinical biomarkers and bioanalytical activities for pre-clinical and clinical drug development.
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Serve as a principal level Biostatistician, working effectively with interdisciplinary teams to contribute strategically (through innovative ideas or applications) to drug development and commercialization at the study and drug compound/therapeutic areas levels.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Responsible to work on Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post-market clinical follow-up (PMCF), Summary of Safety and Clinical Performance (SSCPs), state of the art (SOTA) on medical devices, post market surveillance reports, Periodic safety update reports, Literature reviews, Protocol development, Clinical study reports, and Investigator’s brochure, Clinical Evidence Summaries, Risk-benefit analysis reports for medical devices as per MDD and MDR requirements.
$50 an hourFull-timeExpandApply NowActive JobUpdated Yesterday
and development jobs in Neshanic Station, NJ
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