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As a Barclays US Basel IV Regulatory Capital Reporting Assistant Vice President (AVP), you will be working in the Regulatory Capital Team and will be tasked with the development and on-going circulation and reporting of both point in time and Comprehensive Capital Analysis and Review (CCAR) Projected risk weighted assets (RWAs), capital leverage, and Single Counterparty Credit Limits (SCCL) Large Exposures for Barclays IHC (Intermediate Holding Company) to internal and external stakeholders.
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Maintain and utilize current knowledge of ophthalmic ICD-10, Medicare, HCPCS, third party payor and CPT coding and compliance issues to meet practice objectives. Oversee and manage execution by Office Managers of daily operations of divisional practices including patient access-schedule and flow, financial planning, analysis & reporting, revenue cycle, credentialing, provider relations, MIPS, clinical & surgical services, and optical departments.
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Strong experience with the contents and implementation of specific regulatory initiatives such as: Dodd-Frank, general consumer compliance, regulatory structure and organizations including the FRB, the CFPB, the OCC, the CFTC, FINRA, and the SEC.
$80,550 - $147,675 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions. BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience.
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Experience with CMC regulatory documents (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents) Experience in developing CMC regulatory strategy. These submissions include health authority briefing packages, IND/CTA, BLA/NDA and MAA regulatory filings.
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Ensures cross-functional execution of the pediatric segment strategy with US partners, including sales, brand marketing, customer operations, market access, medical affairs, policy, communications, Health Economics, regulatory, legal, and compliance.
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This position is onsite and has opportunity for growth The Senior Indirect Tax Accountant will be responsible for the accurate and timely filing of all US indirect tax compliance, including sales & use tax, personal property tax and US regulatory taxes.
$98,000 - $131,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsibilities: Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions. Experience with CMC regulatory documents (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents) Knowledge of FDA, EMA and/or ICH guidelines and CMC regulations Experience in drug development processes and post-approval requirements Experience in developing CMC regulatory strategy Experience in project management Have a solution-oriented approach to problem solving Ability to plan/prioritize work of group members and guide/develop others.
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Review professional liability claims and conduct liability assessment in collaboration with the Claims Team. engage in policy review to ensure operational effectiveness and regulatory compliance; support risk management team members with managing issues to ensure compliance with hospital licensing standards, hospital policies and procedures and other regulatory requirements; assist with medical staff professional review activities and compliance with state and federal reporting requirements.
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Job Summary:The Site ECM maintains the site’s export compliance program and is responsible for all aspects of the site’s export compliance activities, including adherence to Group and local policies and procedures, export licensing, auditing, training, and issue investigation, escalation and resolution.
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In-depth knowledge of regulatory compliance in pharmaceutical marketing. Navigate the complex regulatory landscape of pharmaceutical marketing, ensuring all digital content is compliant with industry standards and regulations.
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5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience. Responsible for the global regulatory evaluation of CMC change controls with supervision. 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience.
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Manage all vendors for regulatory activities, pharmacovigilance, state licensing, and compliance. The Associate Director of Regulatory Affairs & Compliance position at IBSA Pharma Inc. will have primary responsibility for the oversight and management of Regulatory matters related to IBSA commercial and development product portfolio.
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CMC regulatory compliance: Communicate and interpret new regulations or regulatory guidance and assess impact of changes. Direct experience with all types of CMC regulatory documents and sections (INDs, NDA, BLA, supplements, and responses) in eCTD format.
$174,000 - $254,150 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Senior Indirect Tax Accountant will be responsible for the accurate and timely filing of all US indirect tax compliance, including sales & use tax, personal property tax and US regulatory taxes (filings undertaken by 3rd party providers.
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medicare compliance regulatory reporting jobs Title: compliance specialist Company: Metroplus Health Plan in Whippany, NJ
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