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Our professionals provide advisory and implementation services that integrate risk, regulatory, and technology skills to help clients transform their legacy programs into proactive cyber risk programs.
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We have an immediate need for a QA Supervisor to oversee aspects of Quality including: QA/QC, Regulatory Compliance and Food Safety - it's a huge opportunity to make an impact! We have an immediate need for a QA Supervisor to oversee aspects of Quality including: QA/QC, Regulatory Compliance and Food Safety - it's a huge opportunity to make an impact.
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We have four main divisions within AH - a full-service Association Management Company; a Marketing and Communications Agency (MarCom); a Meetings & Events Management Team; and a division that focuses on other custom solutions such as strategic planning, website builds, database integrations, accounting services, staff recruitment, credentialing management, public affairs and lobbying, and growing non-dues revenue.
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Supports Regulatory affairs in providing content and providing review of documents supporting CDx submissions to the FDA and other health authorities globally. + Provides scientific and technical expertise by collaborating closely with Translational Science Leads, Clinical Biomarker Leads, Biosample Operations, Clinical Leads and Regulatory Liasions to ensure sucessful implementation of CDx and data collection.
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Partner with the department chair and Senior Associate Dean, Office of Faculty Affairs on faculty development. This role entails the day-to-day management of the academic primary care practice, including ten providers across two sites (Temple Pediatric Care; TPC) and the Well Baby Nursery at Temple University Hospital (TUH.
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Must have national accredited wound certification (CWS, CWCN, WCC, CWON, WOC, AWCC)or be committed to complete Advanced Wound Training and national accredited Wound Certification within 1 year of hire (For those hired with wound certification, completion of a fast-track hybrid program for regulatory wound care requirements will be provided) *Knowledge and experience with clinical charting, incident reporting and investigation response is required.
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Interaction: The Clinical Education Manager may have contact with internal colleagues in compliance, regulatory, pharmacovigilance, marketing, sales, training, research and development, strategy and portfolio management, and HOVA. This internal collaboration is considered a fundamental and essential part of the position.
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Interact with key stakeholders such as Formulation and Process Development, MSAT, Manufacturing, Engineering, and Regulatory Affairs to ensure that Clinical/Commercial Drug Substance/Drug Products are manufactured in accordance with established procedures, cGMPs, and appropriate regulations.
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Leidos QTC Health Services is seeking a Medical Case Specialist to support our Veteran Affairs Operations. As a Medical Case Specialist, you will work closely with veterans and the Veterans Administration to gather, collect, record, track and verify data and information from multiple sources.
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We are PASSIONATE about our country’s veterans, UNITED as a team and INSPIRED to make a difference. Leidos QTC Health Services is the nation’s largest provider of disability and occupational health examination services.
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Collaborate with senior leadership to ensure compliance with external regulatory bodies such as HRSA, FTCA, Joint Commission, and the National Committee for Quality Assurance. § Monitor regulatory sources to stay informed of rapidly changing rules and regulations that relate to credentialing processes.
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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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Director, Global Regulatory Affairs, Precision Medicine. Associate Director, Global Regulatory Affairs Labeling. Associate Director, US Advertising and Promotion, Global Regulatory Affairs.
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Works effectively and collaboratively with a wide range of internal stakeholders from CRLTC sales teams to 340B Center of Excellence, Credit, Finance, Health System sales teams, Regulatory & Compliance, etc.
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Under the supervision of the Head of Government Affairs, help to support U.S. CEO in his role as PhRMA Board Member. - Provide expertise to Government Affairs Public Policy team to identify mitigations and opportunities to shape legislation, proposed rules, and draft guidance.
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regulatory affairs jobs Title: intern Company: Amgen in Levittown, PA
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