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Contribute to Running the Business: Leveraging expertise gained through change the business initiatives support on various legal and regulatory topics (foreign agent registration, anti-trust, ESG, NDAA, conflicts management export control, AI, AB&C, and lobbying.
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You will play a critical role in the Regulatory & Compliance Platform and Corporate Center of Expertise (COE)'s approach to solving existing and emerging regulatory and compliance challenges, including but not limited to regulatory topics such as foreign agent registration, anti-trust, ESG, NDAA, export control, AI, AB&C, and lobbying.
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Proven ability to act as a forward-thinking leader, capable of planning ahead and identifying strategic pathways in regulatory operations. Drive continuous process improvements that enhance both the productivity and strategic alignment of regulatory operations.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Experience and familiarity with inquiries and investigations from the Securities and Exchange Commission (SEC), Department of Justice (DOJ), Commodity Futures Trading Commission (CFTC), State AGs or State Securities Divisions, and Financial Industry Regulatory Authority (FINRA is preferred.
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Experience in leading the preparation of high-quality CMC regulatory submissions (Module 2 and Module 3) for global marketing and post-approval applications. Must have 3-5 years pharmaceutical industry experience (small molecule) in CMC Regulatory Affairs.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Knowledge of CMC regulatory requirements for biologics and small molecules during development and post-approval, including biologic upstream and downstream processes, analytical methods, and drug/device combination products.
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You will lead CMC-regulatory activities listed above with cross-functional teams and act as the regulatory CMC liaison between CMC, regulatory affairs and/or program management, as applicable.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Pykus is seeking a qualified, self-motivated individual to work as a Director of Clinical and Regulatory Affairs in an exciting, fast-paced environment to help advance the development of transformative medical devices that solve well recognized yet unmet needs that enable improved outcomes and patient satisfaction in ophthalmic surgery.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Specialist will be responsible for ensuring that the company complies with all regulations and laws pertaining to its business. Job Title: Regulatory Affairs Specialist.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Stress Testing, Regulatory Reporting, Interest Rate and Liquidity Risk Reporting, Market, Operational and Credit Risk Reporting. You will play a pivotal role in being responsible and guiding our clients to design and develop solutions related to the evolving regulatory compliance landscape within the Financial Services industry.
$326,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The US Director*, will report to the Vice President Regulatory Affairs and will be a core member of a small but agile regulatory team. As a member of the regulatory affairs team your key responsibilities will be to support/co-lead the NDA for our most advanced asset in close collaboration with the cross functional Pritelivir project team.
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Under supervision of Regulatory Strategy Director, prepare and check documents for IND clinical amendments for accuracy and completeness. 1-3 years’ experience in the biotech/pharma industry of which at least 1 year drug regulatory affairs or supporting clinical operations.
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Senior Director, Global Regulatory Affairs Development Pipeline. Supervision of vendors active in regulatory affairs on behalf of BioNTech. Regulatory Intelligence: Monitor changes and evolution in the regulatory landscape for therapeutics and/or diagnostics; analyse the impact of drug/devices changing regulations for BioNTech's products; collect, evaluate and disseminate relevant regulatory updates on competitors' developments.
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We are seeking a highly skilled and experienced Vice President and General Manager for our Blue Sky Regulatory Services (BSRS) business unit. Expertise in the US regulatory filing/ Blue Sky industry.
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The Senior Manager/Associate Director of Regulatory Affairs reports to the Executive Director, Regulatory Affairs and will be responsible for contributing and delivering global regulatory strategies for product development and approval in alignment with the corporate strategy for Stoke’s portfolio.
Full-timeExpandApply NowActive JobUpdated 18 days ago
Title: regulatory Company: Flybreeze in Woburn, MA
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