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The successful candidate will play a key role supporting insurance advertising legal review of carrier collateral and distribution agency collateral, insurance producer commission agreements, marketing content creation, regulatory affairs and litigation management, and also support lead generation and consumer contact.
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Visa is seeking a proactive, business-minded lawyer to join its growing Global Risk & Regulatory Affairs team. Support the Regulatory & Risk Governance team with regulatory engagements.
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The major responsibilities for this position are to work with university faculty and industry partners to develop online, asynchronous content for four Quality Assurance and Regulatory Affairs courses that will lead to a certificate, create in-person experiential learning activities with input from industry hosts, and teach at least one online, asynchronous class each semester once the Quality Assurance and Regulatory Affairs Certificate Program launches in Fall 2025.
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Since being founded the team has seen phenomenal and sustained organic growth, working across Medical Affairs, Publications, Promotional, Commercial and Regulatory spaces for their roster of blue-chip pharmaceutical companies and biotech's.
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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
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COGA’s Senior Director of Legislative and Regulatory Affairs leads legislative efforts and directs outside lobbying firm. COGA’s Senior Director of Legislative and Regulatory Affairs, along with other internal staff and contractors, leads key regulatory efforts and engages at all levels with state regulatory agencies.
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Ensure Compliance: Collaborate with Quality Assurance, Regulatory Affairs, and other cross-functional teams to ensure compliance with industry standards and company policies. Regulatory Knowledge: Knowledge of current FDA regulatory and ISO requirements and trends affecting medical device software.
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The Executive Director, Regulatory Affairs will develop and execute global regulatory strategic and tactical guidance for the development of innovative new drugs in rare disease ensuring fast to market global product registrations, product promotion, maintenance of products and processes in regulatory compliance with local regulations.
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Work closely with the government affairs team to ensure that committee and coalition efforts align with the association's legislative and regulatory priorities. Serve as liaison between Government Affairs Committee/Executive Director and each relevant committee, forum, and coalition to gather input, serve on stakeholder meetings and/or testify on proposed and/or introduced state legislation as needed.
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Serve as internal medical and scientific resource to assigned therapeutic areas for development of disease-state and product communications and materials that are medically accurate, balanced, and consistent with regulatory guidelines.
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Regulatory affairs, drug development understanding is highly preferred. The Business Development Sales Professional at Cardinal Health Regulatory Sciences is a highly sophisticated position that will generate and drive new business opportunities within a myriad of markets.
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6 months to 5 years of experience in Regulatory Affairs of a Consumer Products Company with working knowledge of U.S. FDA labeling regulations as published in 21 CFR Parts 1-199. Vaco Boston has partnered with our client to hire a Regulatory Specialist to join their team.
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Coordination: provides support for OpCo Presidents, Resource Planning, Regulatory Affairs, Corporate Strategy, Environmental Policy and Services, State Affairs, Legal, etc. With partnership with both ISP and Operations, is involved in all stage gate and capital budget process including scope and budget approval, financial authorization, engineering, design and regulatory permitting, construction and project closeout.
$226,166.66 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Provide support, mentorship, and guidance to regulatory affairs and quality assurance to ensure staff can independently make sound strategic and tactical decisions. The mission of the Regulatory Affairs and Quality Assurance team is to empower Cleerly to bring new, safe, and effective products to market and implement a quality foundation to support a patient-focused, innovative heart care organization.
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Delivers timely, accurate, and succinct clinical and scientific presentations to KEEs and HCPs, both proactively and in response to requests for information, consistent with promotional compliance, PhRMA guidelines, and FDA regulatory requirements.
$240,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 19 days ago
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