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This position will work collaboratively with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations.
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Assist the Director of CQR in preparing for and maintaining a continuous state of readiness for regulatory and accreditation preparedness including HRSA, PCMH, DOH, and others as assigned. Manages and oversees QAPI activities including patient experience surveys and reviews, clinical quality measure satisfaction (UDS measures, HEDIS measures, Annual Wellness Visits), pursuant to HRSA and PCMH requirements, value-based care agreements, pay for performance and other population health initiatives.
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Experience working within regulatory standards and requirements such as SOX, HIPAA, GDPR, HITRUST is preferred. Minimum 5 years of experience in IAM with proven expertise in key IAM technologies like OKTA, Siteminder, Sailpoint IIQ, or CyberARK preferred.
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A licensed Pharmacist themselves, the District Leader, Rx brings deep knowledge of pharmacy workflow and clinical programs to help their teams identify and address performance opportunities, grow the top-line through the delivery of clinical services, and abide by all legal and regulatory guidelines with safety of our colleagues and patients top of mind.
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PCG's Health practice offers in-depth programmatic knowledge and regulatory expertise to help state and municipal health agencies respond to regulatory change, improve access to health care, maximize program revenue, improve business processes, and achieve regulatory compliance.
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Penn State Harrisburg's School of Public Affairs invites applications for a non-tenure line position at the rank of Assistant Teaching Professor of Homeland Security and Public Policy starting in fall 2024.
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Monitoring all charts, gauges, and other operating equipment at treatment plant(s) or within the distribution system, utilizing SCADA. Preparing and submitting routine state and regulatory reports for review.
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The Pennsylvania Director of State Affairs serves as the principal staff for state government affairs and chief lobbyist in Pennsylvania, representing the Alzheimer’s Association before Pennsylvania’s legislature, governor, relevant state agencies, community stakeholders and coalitions, and on statewide task forces and work groups.
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Assist facilities management team in ensuring required regulatory permits are acquired, required reports are submitted to regulatory agencies and any site permit conditions (e.g. recordkeeping, process safety management (PSM), stormwater, special waste, etc.
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Expert-level of knowledge of the biopharma industry, including in-depth understanding of other adjacent functions to regulatory (i.e. clinical, pharmacovigilance, quality, medical affairs), as evidenced by proven track record of leading organizations and teams to achieve strategic initiatives relating to digital capabilities.
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May assist with Regulatory Audits by performing first coding review and ranking of charts. This job will deliver value to the Health Plan and its beneficiaries enrolled in Risk Adjusted government programs such as Medicare Advantage (MA) and/or Affordable Care Act (ACA) using skills including butnot limited to Hierarchical Condition Category (HCC) Coding, medical coding, clinical terminology and anatomy/physiology, and Centers for Medicare and Medicaid Services (CMS) coding guidelines.
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Leads business requirement process and reporting to ensure proper and timely notification of case activity to the appropriate regulatory and/or law enforcement agency. Health Care Anti-Fraud Associate (HCAFA) designation.
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Build effective partnerships with all internal stakeholders, including regional and global medical affairs directors, other medical communication leads, HEOR, RWE, biostatistics, clinical development, Early Development, medical science liaisons, medical information, and other members of the publications team.
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5 years of sales and marketing and/or actuarial experience in the areas of health insurance, Medicaid or Medicare managed care plans and/or government affairs (lobbying) 5-7 years of experience with government affairs.
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As a GSK Medical Data Scientist you will have the opportunity to grow your data scientists skills by analysing a variety of disparate data sources (including structured and unstructured data ) and build innovative machine learning algorithms to uncover powerful analytic findings at a customer level that drive data-driven decision making for Medical Affairs strategic planning and execution.
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regulatory affairs jobs Title: sr regulatory affairs associate Company: Thermo Fisher Scientific in Harrisburg, PA
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