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Work closely with internal teams such as clinical research, regulatory affairs, marketing, and sales to integrate alliance activities with overall business goals. The Alliance Manager, Medical and Scientific Affairs for Beckman Coulter Diagnostics is responsible for developing and maintaining strategic partnerships with external organizations, including academic institutions, healthcare providers, government, and industry partners.
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The analyst will regularly work with senior members of Customer Operations, Regulatory and External Affairs, Transmission Operations, Finance, Accounting and outside consultants in performing these daily responsibilities and supporting strategic initiatives.
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JOB SUMMARYUnder the direction of the Director of Licensing and Regulatory Services, provides legal support to in-house counsel, home health, hospice, home care, and senior living operations as part of a dynamic in-house legal department.
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Provide regulatory guidance, general issue management and strategic stakeholder engagement support to Corporate Affairs and business leaders. Reports to the VP, Strategy & State Affairs-Corporate Affairs Administration.
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Key Responsibilities The Medical Science Liaison (MSL) is a member of a field-based team of scientists who function as an extension of the US Medical Affairs organization. MSLs provide medical information through scientific exchange in a fair-balanced manner and provide clinical/scientific support for Bristol Myers Squibb and the Medical Affairs department at the direction of Medical Affairs management.
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Experienced HireShift 1 (United States of America)US, Washington, D.C.Intel’s Legal, Trade, and Government Affairs (LTG) group offers unique opportunities to work in a variety of areas, including counsel to Intel businesses; technology and intellectual property licensing; patent prosecution; trademarks and brands; litigation, mergers, acquisitions and investing; public policy, legislative and regulatory lobbying; global trade, export, import, and customs; and corporate compliance.
$162,600 - $284,620 a yearExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Support Hoxworth Blood Center’s safety, cGMP, and Quality Plan in coordination with the Division Director, Quality and Regulatory Affairs. It ensures effective qualification, use, maintenance, calibration, and repair of medical equipment used in the provision of blood, blood components, tissues, and derivatives in accordance with safety standards and regulatory requirements.
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Regularly interfaces with team members in R&D including Biostatistics and SAS Programming staff, Data Management, clinical research and operations teams, regulatory affairs, clinical pharmacology, medical writing, medical affairs and quality management.
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The College is based in one of the largest integrated academic health centers in the country, with Colleges of Medicine, Nursing, Dentistry, Public Health and Health Professions, and Veterinary Medicine, as well as the UF Health and the Veterans Affairs Medical Center, situated on a campus serving over , students.
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The Market Risk Regulatory Policy Manager will be responsible for leading on the development of a full library of policy interpretations which lay out Company’s approach to aspects of the US FRTB rules which may be silent or ambiguous.
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Assist in the preparation and drafting of testimony, regulatory comments, and position statements sent to legislative and regulatory bodies and other interested parties concerning legislation, policies, published reports, regulations, and statutes governing Medicaid, long-term services and supports (LTSS), and other waiver programs.
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Works collaboratively with Risk, Legal, Billing and Regulatory Compliance, Accreditation, and Regulatory Affairs leadership to comply with state and national norms of legal and regulatory health care compliance.
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Exercise product risk management related to ADTS activities (, technical recommendations), Product Stewardship and Regulatory affairs. Good interpersonal skills, open to listening and sharing experiences, effectively communicating project goals/objectives, collaborating, and maintaining good working relationships with co-workers in cross-functional teams.
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The Senior Director of Adcovavy & Legislative Affairs represents CHS before the Florida State Legislature, Governor's Office, state agencies, advocacy groups and the public to advance CHS interests and funding, positioning CHS as the leading resource for public policy that positively impacts the lives of children in Florida.
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Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. But working at Bristol Myers Squibb is anything but usual.
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regulatory affairs jobs Title: regulatory affairs project manager Company: Gpac
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