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Strong knowledge of and/or experience with government programs regulatory, operational, financial, and clinical requirements for the delivery of health insurance and managed care products and services, including Medicare, Medicaid, MMP, LTSS, SNP, Duals, CHIP, and behavioral health, as well as the associated and relevant federal, state, and local regulatory entities.
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As a pivotal leader within the Division of Student Affairs, the Director of Residence Life reports to the Senior Associate Dean of Students and oversees a large and multifaceted residential program.
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Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Ensure laboratory is compliant with corporate, state and federal regulatory requirements (CAP, CLIA, State, ISO, etc) related to personnel safety and quality of laboratory testing as well as professional conduct.
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A thorough understanding of global drug development functional areas including preclinical, clinical, regulatory affairs and manufacturing. Knowledge of GLP/GCLP and GCP global regulatory requirements for clinical trial submissions (USA, UK & EU), understanding of 21CFR Pt. 11 with respect to clinical systems (QMS.
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As our Senior Business Performance Analyst, at ENGIE’s Medical Area Total Energy Plant (MATEP), you will be responsible for MATEP’s operational reporting, including internal and external reporting of regulatory compliance and plant financial information, supporting budgets, forecasts, and operating results.
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We work on a wide variety of technologies including AWS, Oracle, Snowflake, Angular, Java, Spring Boot, Python, REST/API, Kafka, and Tableau.
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Understanding of regulatory requirements and frameworks such as HIPAA, PCI-DSS, and NIST. Ensure CyberArk implementations comply with internal security policies, standards, and regulatory requirements.
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Deep understanding of how capital markets function including market structure, key operational functions, and regulatory constructs. We assist companies and non-profit organizations in delivering benefits to their employees.
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Preferred knowledge in thermal analysis, X-ray powder diffraction, contributions to synthetic chemistry, and regulatory documentation. Proficient in organic chemistry tools (HPLC, LCMS, GC, NMR) and software (ChemDraw, Excel.
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This individual will ensure timely, consistent, and accurate safety reporting in accordance with FDA, EMA, and ICH guidelines, applicable regulatory requirements, Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and best practice, scalable, standard operating procedures (SOPs.
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Familiarity with regulatory requirements and compliance in equity capital markets. This is a brand-new role for the firm, reporting to our CO-Chief Investment Officer and will offer an exciting opportunity to become a pivotal partner in shaping our equity capital markets strategy.
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Support compliance with antitrust regulatory reporting obligations. Monitor and respond to relevant antitrust developments and regulatory trends across the globe. The ideal candidate will have at least 7+ years of relevant experience in a top law firm and/or in-house antitrust work.
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Responsibilities of the Medical Laboratory Technologist-Histocompatibility:Monitor lab performance/regulatory compliance/final review of daily, weekly, monthly, and annual surveillance documents.
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We are a human-centered group that partners with our clients to provide expert HF consulting services, whether it’s delivering an entire usability engineering program alongside device development teams, guiding clients on HF regulatory strategy, providing HF advisory support to our in-house teams, or conducting generative, formative, validation, and comparison studies.
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This includes: an industry-leading dispatch management platform powered by Swoop; comprehensive accident management services; knowledgeable consumer affairs and connected vehicle capabilities; and a growing marketplace of services, discounts and support enabled by a robust partner ecosystem.
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regulatory affairs jobs Title: principal consultant Company: Parexel in Cambridge, MA
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