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Engage with regulatory agencies and industry stakeholders regarding regulatory and legislative affairs, including by providing feedback on proposed regulations. 2+ years' experience working in regulatory compliance or regulatory affairs for a consumer products, food, beverage, cosmetics or pharmaceutical company, or in a highly regulated industry.
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Internal stakeholders include: VP Immunology, International Market Access and Pricing; Global Health Economics and Outcomes Research; Affiliates; Areas; R&D; Commercial; Medical and Regulatory; Governance bodies.
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The FHCC is a first-of-its-kind partnership between the US Department of Veterans Affairs and the Department of Defense (DoD), integrating all medical care into a federal health care facility with a single combined VA and Navy mission: "Readying Warriors and Caring for Heroes.
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The applicant is expected to develop highly effective collaborations with relevant stakeholders including those in Patient Health & Impact, the Patient-Centered Outcomes Assessment Group, Statistics, Clinical Pharmacology, Clinical Development, Medical Affairs, Epidemiology, Programming, and other groups contributing to HEOR analysis and strategy.
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You will work across businesses and across functional groups including Global Marketing, Market Access , Research & Development, Medical & Scientific Affairs, and Finance. Thorough understanding of global guidelines as they relate to HEOR and Medical Affairs, as well as expertise in global HTA/payer reimbursement and market access requirements.
$143,300 - $286,700 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This position is located within the Captain James A. Lovell Federal Health Care Center in North Chicago, performing law enforcement work for the preservation of peace and the prevention, detection, and investigation of crimes occurring on Department of Veterans Affairs (VA) controlled property.
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AbbVie's Digital Science Team is a novel capability team bridging medical, scientific, technology, regulatory, and data science expertise to deploy digital health technologies (DHTs) into our studies.
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Oversee consultants providing biostatistical and scientific writing support for Medical Affairs, Regulatory Affairs, and Marketing initiatives. We currently have a great opportunity available for a Medical Scientific Affairs Manager - SII. The Manager of Medical Affairs will play a pivotal role in supporting our clinical study portfolio and spearheading the generation of scientific evidence and publications.
$125,000 - $138,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Develop and implement medical policies and procedures to support business, legal and regulatory needs including but not limited to donor advisement and medical affairs guidance (MAG). Provide medical expertise to various BPS departments such as Operations , Legal , Regulatory , Quality Assurance, IT, Marketing and Environmental, Health and Safety (EHS.
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Interface with EHS to maintain compliance with OSHA and other regulatory agencies, and act as the principal investigator for selected IND studies performed in BPS-US facilities. Overseeing all Biolife (BPS ) Medical Affairs.
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Assist in the development of key strategic communications and presentations to a broad range of stakeholders including Board of Directors, Executive Committee, Management Committee, ALCO and Balance Sheet Committee, Rating Agencies, and Regulatory Agencies.
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Do you have 3+ years of experience in regulatory affairs, and do you have experience in labeling / preparing safety data sheets? Required Knowledge: Regulatory, Scientific / Technical, QA, Business acumen.
$90,000 - $110,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to RD product development design and safety to ensure compliance in all research data collection and reporting activities.
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The Cyber Defense service will be developed with adherence to RCP policies, relevant industry frameworks, regulatory, compliance and operational performance requirements. The Cyber Defense Senior Manager with report directly to the RCP Director of Information Security and provide the vision and strategic direction for building and running Reynolds Consumer Products' new stand-alone Continuous Monitoring, Vulnerability Management, Threat Intelligence and Incident Response programs.
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Obtain Licenses: Become a FINRA (Financial Industry Regulatory Authority) Registered Representative by studying for and obtaining your SIE, Series 7 Top Off and Series 66 licenses, fully paid for and sponsored by Fidelity.
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regulatory affairs jobs Title: assistant Company: Veterans Affairs Health Administration in Mettawa, IL
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