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Experienced attorney (holding a law degree) with 8+ years doing regulatory and/or compliance work in a top law firm and/or in-house legal department. Support AV testing, ridehailing and/or delivery teams in meeting their objectives and ensure compliance with regulatory requirements.
$153,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Regulatory Manager will focus on monitoring and advocating for market policies that will advance the interests of RWECE within the Western interconnect. The Regulatory Manager is a key role within the RWE Clean Energy (RWECE) Regulatory Team working on Wholesale Markets in the West region.
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Lead the planning, execution, and delivery of regulatory programs that are considered the highest priority to Cash App. Lead cross-functional teams (including Product, Engineering, Data Science, Compliance, Counsel, Law Firms, Regulatory Consultants and bank partners) involved in program, providing direction, support, and guidance to ensure alignment with program objectives and timelines.
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Our Client's FDA regulatory group works with broad range of companies, including medical devices, drugs, biologics, diagnostics, digital health, research tools, cosmetics, dietary supplements, wellness products, and other consumer products.
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You will need to work closely with the Vice President, Global Regulatory Affairs Oncology and Precision Medicine, and collaborate with the biomarker team and global/regional regulatory liaisons to provide Precision Medicine global regulatory guidance.
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As a Director, Global Regulatory Affairs, Precision Medicine you will develop and execute Precision Medicine regulatory strategies in alignment with the drug global regulatory strategy in collaboration with cross functional stakeholders across the Gilead therapeutic areas and in compliance with the appropriate regulations.
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The Chief Compliance Officer ("CCO") will act as the primary expert and advisor on all NerdWallet compliance matters, managing external regulatory engagements, legal contracts, and third-party vendor compliance.
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Prepare, review, or edit cGMP batch records, CMC regulatory and Quality documents. The candidate will be responsible for chemical development-related activities across the portfolio including process development and manufacture of regulatory starting materials (RSMs) and support production of Drug Substance (DS) for clinical trial materials, and establishment of associated Control Strategy for RSMs and DS to support NDA/MAA filing and commercial manufacturing.
$200ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Strong knowledge of pharmacokinetics and modeling, pharmacodynamic principles, ADME concepts, bioanalytical principles, regulatory guidelines and clinical pharmacology requirements in late stage clinical development.
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You know how to define and shape a company’s financial, management or regulatory reporting strategy. You’ve worked with these FinTech solutions: Anaplan, Hyperion, BPC, Tableau, Qlik, OneStream.
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Responsibilities include oversight of late development/launch preparation activities including (but not limited to): the development of chemical processes for active pharmaceutical ingredients (APIs) and regulatory starting materials (RSMs), process scale-up, technology transfer, and validation of chemical processes.
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Strong knowledge of model-informed drug development, DMPK-Clinical Pharmacology concepts, and regulatory requirements. From leading clinical pharmacology programs to driving regulatory decisions, your expertise will drive the development and registration of groundbreaking therapies.
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Develops/Reviews Stormwater Management Reports and Stormwater Pollution Prevention Plans (SWPPP) to support regulatory permits; + Conversant with regulatory codes, design codes and standards, best management practices, permit requirements and construction practices.
$93,400 - $155,100 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Identify the need to conduct CEQA/NEPA reviews on projects, acquire environmental resource discretionary permits, complete the application process and negotiate the terms of such permits with the regulatory and land management agencies.
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Strong understanding of Registered Investment Advisors (RIA) structures, concepts, needs; key regulatory bodies, and how modern clearing, custody, and brokerage platforms fits into the capital market ecosystem.
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regulatory job Title: sr Company: Csl Behring in South San Francisco, CA
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