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The Manager, Medical Affairs & Grants manages the extended Grants team associates, system administrator & project manager to assure timely and compliant processing of educational and charitable grants, donations and fellowship applications, for six Medical Device Business Units, including Cardiac Rhythm Management, Electrophysiology, Heart Failure, Structural Heart, Vascular, and Neuromodulation.
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The MAM will identify and collaborate with HCPs to amplify clinical data, improve educational efforts, promote the proper use of therapies, and provide strategic insights to BSC. Additionally, the MAM will work with senior management at BSC to align priorities and act as a liaison between Clinical Affairs, Marketing, R&D, and Program Management.
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At least four years of government affairs, legislative, lobbying, regulatory, or public policy experience. Coordinates government affairs initiatives and efforts with sustainability, regulatory compliance, and import/export functions within the company.
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Work with Regulatory Affairs staff, engineers and technical experts to resolve potential regulatory issues, deficiencies and questions from regulatory agencies. Job Family Regulatory Affairs.
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Senior Regulatory Affairs Specialist. You will design, build, implement, and sustain world-class regulatory affairs recommendations, decisions, and submissions while employing working knowledge of global regulatory requirements.
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Political Affairs Internship: The role focuses on making poverty a focus of U.S., Canadian and U.K. foreign policy. Political Affairs Internship: The role focuses on making poverty a focus of U.S., Canadian and U.K. foreign policy.
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Develop and ensure execution of impactful medical affairs strategy and tactics for HQ and Field teams to support product development, pre- and post-launch activities as aligned with the SVP, Chief Medical Officer.
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Position Summary: The Advanced Regulatory Affairs Specialist provides independent support to senior regulatory staff to submit regulatory filings. Qualifications Education and Experience: Bachelor's degree with 3-5 years of relevant experience in regulatory affairs in an IVD manufacturing environment; Or, a master’s degree with up to 2 years of relevant experience Knowledge, Skills, and Abilities: Excellent attention to detail and organizational skills are required.
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The Postal Affairs Manager is responsible for overseeing all aspects of postal affairs management, including compliance with postal regulations, optimization of mailing strategies, and coordination of mailing campaigns.
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Our client, a leading player in the pharmaceutical industry, is renowned for its collaborative and transparent environment.
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Abbott is seeking a passionate, experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, or St. Paul, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems.
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This position is part of Quality and Regulatory Affairs located in Fargo, ND and will be fully remote. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance with global regulations and standards across multiple markets.
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The Head of Corporate & Legal Affairs will report directly to the CEO, with whom Cornerstone has had over a decade-long relationship and is a well-respected, collaborative leader with a rich history of working for start-ups and well-established CROs.
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The Regulatory Affairs Specialist will support international registrations and renewals. Laborie Medical Technologies is currently searching for a Senior Regulatory Affairs Specialist to join our team.
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As a Director, Regulatory Affairs , you will use your expertise to lead and mentor a team of high-performing Regulatory Affairs professionals; provide invaluable strategic, technical, and regulatory advice to help clients with their various innovative product applications; and manage client relationships.
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Title: affairs in Robbinsdale, MN
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