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Insmed is seeking an innovative and highly motivated senior scientist to support development, production, and characterization of novel AAV gene therapies at the New Jersey Research Development Labs. Responsibilities may include AAV production and purification, AAV potency testing, AAV titration, and AAV transgene construct design.
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Our partnership with Rutgers University creates the state's largest academic healthcare system dedicated to providing high-quality patient care, leading-edge research, and world-class health and medical education, further advancing our mission of providing high-quality healthcare in New Jersey.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Work From Home, Entry Level Data Entry Clerk As A Research Participant. We need folks who want to do tasks, micro tasks, work at home opinion panels, online focus groups, product testing, research trials and more.
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The research program is supported by a dedicated full time epidemiologist/biostatistician and a dermatology specific informatics program. The research portfolio of the Dermatology Service includes optical engineering, artificial intelligence, basic science, translational science, epidemiology and clinical trials with over $5 million of annual funding from NIH, Foundations, Industry, and philanthropic sources.
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The primary focus of the Senior Research Associate – Attributes role will be to build CAR/TCR T cell product and process understanding in support of early and late-stage CAR T with a particular focus on exploratory/investigational needs for mid-stage programs.
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Provide statistical expertise for design, analysis and reporting of clinical or scientific research studies or programs and contribute to development of modern program/trial design methodologies with a focus on real world evidence (RWE) gathering, analysis and interpretation.
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Extensive experience in medical affairs/post-approval area and execution of project user requirements, system design, validation plans, operational and performance protocols, research, and development of applications and toolkits for end-users.
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Perform analytical research in support of the Compliance Department, with a strong focus on AML/BSA, including the design, development, and implementation of information-based business solutions.
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Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed. Able to handle a variety of clinical research tasks. 5+ years of experience for a Manager role or 10+ years of experience for the Associate Director role in data management in either a CRO/or pharmaceutical or biotech industry or equivalent relevant experience and/or demonstrated competencies.
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Conduct comprehensive research on ESG trends, regulatory frameworks, and best practices across various industries in support of sustainability strategy and related initiatives; deliver decision-useful information to senior management and provide valuable insights to our program.
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12 years or more experience in the CRO/pharmaceutical industry, including experience at Director level, with a proven track record in securing and winning new business, or alternative combination of research and CRO experience and demonstrated competencies in the key requirements for the role.
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Experience working with Citrix Provisioning Services (PVS) and Citrix Machine Creation Services (MCS) Experience working with Citrix User Profile Manager (UPM) and Profile Unity (ProU) Experience working with various hypervisors, such as VMWare and Acropolis Experience installing, updating, and working with Citrix Enterprise Layer Manager (ELM.
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Oversee medical safety and pharmacovigilance activities conducted in partnership with external business partners or outsource to vendors and contract research organizations (CROs). Provides medical expert safety review input into all critical documents for clinical development of products (e.g., protocols and amendments, ICFs, IBs, IMPDs, clinical research reports, INDs, CTAs.
$339,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Proactively track and analyze elements and variables to identify ways to improve the product As an Angular UI Developer, you can look forward to:Working with one of the market leaders in design driven thinking and development, evolving, and building market leading wealth tech product user experience.
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user research jobs Title: director Company: Hackajob in Basking Ridge, NJ
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