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Independently provide complex technical support of cGMP manufacturing including authoring of complex technology transfer documents, change controls, manufacturing impact assessments, and study protocols.
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Applies quantitative skills, via modeling and simulation, to provide dose selection and complex issues at various stages of drug development. BS/BA degree in clinical pharmacology, pharmacokinetics, pharmacometrics, mathematics, engineering, computational biology or a related field required plus at least 14 years of relevant experience.
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Desired skills include:Experience designing and/or fabricating micromechanical devices and systemsAbility to develop creative solutions to complex systems problems by leveraging novel MEMS device development, nuclear physics, materials, optics and related technologies.
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The Maternal Health team is building upon these assets and connecting dots across businesses to create unified and differentiated maternal health solutions all in service of helping our customers tackle their most complex maternity care challenges.
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Expert knowledge and working experience of the USPTO Patent Center filing system in order to independently draft and prepare simple to moderately complex patent legal documents for submission to the USPTO including (but not limited to) patent applications, figures, sequence listings, amendments, information disclosure statements, office action responses, requests for continued examination, notices of appeal, reply briefs, allowance checklists, allowed claims, issue fee payments, etc.
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What sets you apart: Experience defining verification methodology for complex FPGAs∯*∯ Ability to analyze requirements, create test plan, build and set up scalable simulation environments from the ground up using SystemVerilog/UVM Familiarity with testing complex designs, code coverage, functional coverage, assertions.
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MS/MA degree in clinical pharmacology, pharmacokinetics, pharmacometrics, mathematics, engineering, computational biology or a related field required plus at least 12 years of relevant experience. Ph. D. degree in clinical pharmacology, pharmacokinetics, pharmacometrics, mathematics, engineering, computational biology or a related field required, with or without post-doctoral experience plus 5 years of relevant experience.
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Must operate independently and navigate complex regulatory environments in person and via digital channels from remote (non-office based) environment. Effectively mediate KOL's complex and controversial opinions vs; corporate policy decisions ensuring KOL relationships/medical strategy are not negatively impacted.
$140,250 - $187,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Demonstrated experience with innovative assay development and proven ability to troubleshoot and solve complex problems effectively, experience in collaborating with external specialty laboratories.
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Monitors progress of patent cases and patent attorney/agent dockets through use of USPTO Private PAIR, IP Management Software and Document Management System. Performs Patent Term Adjustment review and analysis and delivery of analysis summary to patent attorney/agent.
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The Portfolio Manager will report to the Assistant Director of Research Administration and provide pre and post-award research support for a number of research groups, with complex portfolios, from a wide range of federal sponsoring agencies (e.g. NSF, DoD, ARO, ONR, AFOSR, DARPA, DoE, NASA, NNSA, NIST, NIH and National Laboratories), non-federal institutions and foundations plus internal Harvard funding which consists of startup funds and gift accounts.
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Develop and apply state-of-the-art artificial intelligence/machine learning algorithms, including geometric deep learning and graph-based models, to predict complex biomolecular interactions and their selectivity.
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Perform preparative HPLC using RP and Ion Exchange chromatography techniques to purify and separate complex mixtures of compounds, with a focus on therapeutic molecules and lipid nanoparticles.
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You're the right fit if:5+ years’ experience focused on design, development, testing, and integration of transistor-level IC design and layout of complex mixed-signal circuits and systems-on-chip; RF circuit experience a plus.
$120,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Within their geography, the FRM is responsible for addressing access barriers by strategically working with customers and accounts to solve the most complex patient access issues through all facets of the reimbursement cycle.
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complex job Title: program manager Company: Crowdstaffing in Needham, MA
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