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We invested in new offices, sector teams and practice groups including investor engagement; shareholder activism; governance; regulatory and public affairs, including geopolitical; crisis; litigation; social issues including climate change and diversity, equity and inclusion; cybersecurity, data and privacy; employee engagement; digital communications; opinion research and analysis, and; creative services.
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The Global Scientific Affairs COVID & Flu Senior Manager will play a key role in delivering in-house RWE projects and support the development of Vaccines and Antivirals strategy to keep up with the evolving RWE landscape.
$131,200 - $218,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Ensuring the business remains in compliance with OPWDD, DOHMH and DDD /NJDHS Policies, rule, and all related regulatory agency requirements. Collaborating and coordinating operations with OPWDD and DDD Human Resources Division, Legal Affairs, Labor Relations, Affirmative Action / EEO.
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Collaborate with cross-functional teams, including analytical development, formulation development, quality assurance, and regulatory affairs, to ensure seamless project progression. Own the drug substance modules in the regulatory dossier and collaborate with regulatory affairs to support regulatory submissions and inspections.
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Collaborate with other organizational departments responsible for functional aspects of the HIV Special Needs Plan, including, but not limited to Integrated Care Management, Behavioral Health, Managed Long-Term Care, Utilization Management, Quality Management, Credentialing, Regulatory Affairs, Compliance, Corporate Affairs, Provider Network Operations, Medicare Services, Information Systems, Finance, Claims, and Member Services and Eligibility.
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Our teams include Communications, Community Impact and Investment, Community Finance, CRA Strategy and Program Management, the Government and Political Affairs Group, Regulatory Relations, and Strategy and Engagement.
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Preferably, additional experience in regulatory affairs, medical devices, and RD.Familiarity with global compliance issues, including FCPA, is advantageous. Experience in regulatory affairs, medical devices, and research and development (RD) is highly desirable.
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Degrees in international affairs, political science, or another liberal arts program, as well as in business, finance, or accounting are preferred, but candidates from other backgrounds will be considered as well.
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Support Fubo Corporate Counsel, Legal & Regulatory Affairs and Legal & Business Affairs teams in litigation, regulatory, corporate governance, compliance and transactional matters, including assisting in the review, drafting and tracking of agreements.
$135,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Minimum of 7-10 years of experience in regulatory affairs, compliance, or related roles within the financial services, fintech, or blockchain industry. We are seeking an experienced and dynamic Head of Regulatory Affairs to join our team at Merkle Science.
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Generate research and craft compelling content such as white papers, policy reports, memos, one pagers, legislative drafts, and presentations for external stakeholders; Monitor ongoing regulatory and legislative efforts around relevant issues, such as bond financing, workforce development, outcome based financing models, career pathways, and apprenticeships to ensure Pursuit stays at the forefront of industry developments.
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Our full range of advisory services includes strategic communications, investor relations, financial transactions and restructuring, management consulting, physical and cyber risk, organizational design, board and executive search, geopolitics and government affairs, corporate governance, ESG and DE&I.
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You will work closely with members of the firm's lines of business, Legal Department, Global Government Relations and Office of Regulatory Affairs to help coordinate the firm's response to proposed rules and regulations.
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Review and approval of Clinical Study Protocols, Clinical Study Reports, Statistical Analysis Plans, and ISS.Represent Regulatory Affairs on cross-functional teams. This role reports to CMO.Key Responsibilities:Develop and implement Regulatory Affairs strategies and tactical work plans during clinical development and in preparation for the anticipated US filings.
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Harness your team's market intelligence to bring insights to broader External Affairs, shaping perspectives and informing lending and investment decisions; share intelligence with peers across the company to deepen our shared understanding, promote collaboration, and maximize impact.
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regulatory affairs jobs in New York, Lahaina, Hawaii
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