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Provide to FINRA staff data, information and reporting on a wide range of issues related to the financial products and services marketplace, including regulatory research, regulatory and policy developments.
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We invested in new offices, sector teams and practice groups including higher education; foundations; investor engagement; shareholder activism; governance; regulatory and public affairs, including geopolitical; crisis; litigation; social issues including climate change and diversity, equity and inclusion; cybersecurity, data and privacy; employee engagement; digital communications; opinion research and analysis, and creative services.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Provide clinical documentation using malaria databases, NIH electronic medical records, and regulatory documentation of events post-vaccination. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries.
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Clean Technology, Renewable Energy, Higher Education, Energy Efficiency, Environmental Consulting Services, Waste Management, Water Management, Research, Government Administration, Environmental Services.
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QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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Manage legislative issues to include pending and enacted state legislation and state regulatory activities as specified by the Vice President, State Government Relations. Provide research, information, leadership and deliverables to FMI members, state associations and FMI staff on assigned state government affairs issues of priority interest to the industry.
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The ideal candidate would also have at least two years of experience in one or more of the following practice areas: a) Export compliance, including advising entities involved in transactions with countries subject to U.S. sanctions; b) Antitrust law; c) International law; d) Public utilities/regulatory economics law, e) Complex litigation, or f) Hazardous Materials Transportation law.
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This position will work under the direction of senior staff members to complete historical research assignments that involve the use of libraries, archives, corporate and regulatory agency collections, electronic databases, and other sources of documentary evidence.
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The ideal candidate will have a broad understanding of clinical research, regulatory and policy requirements especially NIH, OHRP, and FDA requirements. Serve as a COR for NIA’s Clinical Research Support Services contract.
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Nonprofit advocacy organization dedicated to saving and improving human and animal lives through ethical and effective scientific research seeks a scientist with a master's or doctoral degree in toxicology, pharmacology, cell biology, or a related field and at least seven years of experience in a nongovernmental organization, government, or industry position related to regulatory testing and/or compliance to promote alternatives to the use of animals in toxicological testing and research.
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Knowledge of Good Clinical Practices (GCP), FDA and EMEA/CHMP regulations and guidelines, and applicable international regulatory requirements. Experience with developing study concepts for clinical development and clinical trial designs with cross functional input, including biostatistics, observational research and patient reported outcomes in Phase 1,2 and/or 3 clinical trials.
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Clinical Research Medical Direct or, Hematology/Oncology - US, Remote. Author CSRs, publications, and regulatory submissions. 2 years of clinical research experience and/or basic science research.
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Research, or supervise the research of, each of statutes, legal opinions, policies, regulations, guidance, case law, and historical PHMSA and Department practice, on matters for which the Regulatory Affairs Law Division is responsible, including those involving complex or high- profile issues of law or policy.
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The majority of the work is regulatory focused, therefore, our Senior Research Analysts also generate evidence for submission to federal regulators at the US Food and Drug Administration (FDA) and European Medicines Agency (EMA), along with occasional interaction with other international regulators.
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research regulatory jobs in Bethesda, MD
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