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As part of the US Medical Affairs team, the Medical Science Liaison (MSL) will be responsible for engaging identified key opinion leaders (KOLs) from institutions and organizations within the assigned geographical territory through high level scientific support for research activities, publications, education, consulting, and other Medical Affairs initiatives.
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Knowledge of Bank Secrecy Act regulatory requirements, including CTRs and SARs, and basic knowledge of banking regulations. BSA Analyst responsibilities include: Administering the Bank Secrecy Act/Anti-Money Laundering Program and related procedures in accordance with Bank’s policies, procedures, and applicable federal regulations.
$70,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Credentialing Manager manages all credentialing functions including application management and primary source verification, ensures compliance with appropriate accrediting and regulatory agencies, supervises credentialing staff, and oversees credentialing workflows and/or services provided by third party vendors as appropriate.
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NET, Angular and JavaScript, SQL Server, AWS (container and sever-less), Git, Visual Studio and/or front-end technologies including CSS, Semantic HTML and Responsive DesigPreferences:Experience with Supervision Regulatory technology solutions coupled with a strong understanding of appropriate metrics and key performance indicators.
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Stay abreast of clinical pharmacology, MIDD, analysis methodology and overall drug development process, including regulatory guidance, and methods in modeling and simulation by engaging with the scientific community (e.g., publishing, presenting at meetings, participating in special interest groups within professional societies, etc.
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Position Summary The Associate Director, Local Government Affairs is responsible for working collaboratively with internal and external stakeholders across the assigned states and home-based sites in the East Region (NJ, MA, FL, PR, NY) to advance BMS reputation and branding in coordination with the USPGA team to advance legislative and regulatory priorities.
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The Field Medical Director, US Medical Affairs will report to the VP of USM Hematology. Represent the US Medical Affairs as a therapeutic expert at ad boards and steering committee.
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At least 1 year in HCC or a compliance related area: monitoring, testing, auditing, finance, compliance, regulatory, law, or a related field. The HCC Program Management Analyst will engage and support the HCC Officers (HCCOs) to provide sustained support and build partnerships with all levels of management, employees, and contractors.
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License to practice Speech Language Pathology issued by PA Bureau of Professional and Occupational Affairs is preferred. Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program.
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Conducts independent examinations, reviews, and related financial investigations of complex cases encompassing all types of financial institutions (FIs) and non-financial trades or businesses (NFTBs) to assure their compliance with statutory and regulatory requirements of Title 31 (Bank Secrecy Act), and Form 8300 filing.
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Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required. The Speech-Language Pathologist (SLP) will access needs, plan strategies and deliver evidence based supports to students with communicative disabilities across a variety of educational settings to include general and special education classrooms, specialized schools and community settings.
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Primarily responsible for federal and state regulatory counsel including but not limited to fraud and abuse, stark law, anti-kickback and HIPAA. 5+ years of experience in Healthcare Regulatory counsel.
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To accomplish this, the Sr. IT Portfolio Manager will maintain and support the development of project portfolio status reporting standards and oversee reporting of their portfolio to IT Leadership on key performance metrics, such as budget and schedule health, risks and mitigation plans, project/product intake, demand, and resource management processes.
$130,000 - $150,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Stays up to date and compliant with the regulatory landscape related to drug safety and data analyses. Minimum of 3-5 years of experience in data analysis, statistical modeling, and data visualization, preferably within the biopharma or healthcare industry.
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Arrow Electronics is looking for an experienced Oracle database, system, ERP EBS Applications and SQL performance tuning expert with an ability to identify, analyze performance issues and provide solutions, workarounds to resolve system performance issues in a fast paced Oracle EBS R12.2 with 50TB of data in a Multinode EBS app tiers and high availability multi node cluster RAC environment.
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regulatory affairs jobs Title: sr director Company: Merck in Trenton, NJ
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