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Job Segment: Environmental Engineering, Risk Management, Law, Regulatory Affairs, Social Media, Engineering, Finance, Legal, Marketing. The Regulatory Manager i s a key role within the RWE Clean Energy (RWECE) Regulatory Team. You will focus on monitoring and advocating for market policies that will advance the interests of RWECE within the Western interconnect.
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This position is housed in the Clinical Research Support Office (CRSO), a centralized clinical trial management office in the UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC), which provides project management and clinical research coordinator staff, and regulatory services for oncology related clinical trials.
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Errors or omissions may ultimately place research participant at undo risk and / or compromise the institution's assurance of regulatory compliance with the federal government. The Cardiology Research Regulatory Manager is a seasoned, experienced research compliance professional with a full understanding of industry practices and organization policies / procedures to apply federal, state, and university regulations, policies, and guidelines, and promote best practices.
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3+ years direct experience with federal regulatory examinations (FDIC, FRB, OCC, or CFPB) and bank partnership lending models. You will work with partners in legal, operations, compliance, finance, data analytics and engineering, product and other teams, to ensure that Block is compliant with applicable requirements and obligations while, to the extent possible, streamlining regulatory impact and facilitating innovation.
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The UPSIDE Foods Global Scientific & Regulatory Affairs (GSRA) team is hiring an Associate Director, Regulatory Operations to proactively create and build effective regulatory compliance operational capabilities.
$185,000 - $205,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The successful candidate will have experience working with clinical trials and their Principal Investigators (PIs), reviewing, and developing clinical trial protocols and consent forms, and have experience submitting to regulatory agencies, including IRB and FDA submissions.
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Regulatory Affairs Specialist – APAC - Diabetes Care (on-site) page is loaded. We are presently hiring for a Regulatory Affairs Specialist, as part of the Regulatory Affairs Asia Pacific (APAC) team, on-site at our Diabetes Care Division HQ location in Alameda, CA. As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
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Lead the migration of existing regulatory documentation to the new Veeva system. The role involves working closely with the regulatory information management vendor (Veeva) to lead the implementation of the Veeva RIM cloud-based software solution.
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Consumer lending product knowledge (e.g., mortgage, auto, credit card, payments), consumer lending life cycle knowledge (e.g., marketing, origination, pricing, risk and servicing), consumer regulation knowledge (e.g., fair lending, CRA, UDAAP, TILA, RESPA), regulatory requirements of the Federal Reserve, OCC, and/or FDIC.
$82,800 - $136,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead implementation of the Veeva RIM cloud-based software solution for regulatory information management. 5 - 7 years of experience in Regulatory Affairs or a related discipline in the pharmaceutical or healthcare industry (preferably with exposure to document control systems.
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CGS comprises an exciting and fast paced team which offers many learning opportunities through exposure to regulatory approval process, asset acquisition, trading, portfolio planning and analytics, risk, compliance, and reporting.
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Responsible for developing global CMC regulatory strategy (e.g., CMC strategy/planning for NMEs), driving global CMC RA related activities and successfully executing regulatory strategies in collaboration with stakeholders.
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You Have:3+ years direct experience with federal regulatory examinations (FDIC, FRB, OCC, or CFPB) and bank partnership lending models. Chief among the role's responsibilities involve full cycle examination management support including managing intake of examination requests, work with partners to obtain responses, facilitate regulatory submissions in the appropriate time frame and manage communications with partners.
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Experience interpreting and explaining legal and regulatory obligations clearly across multiple disciplines and levels. Your mission is to uphold Block's lending obligations in connection with its federal regulatory examinations.
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Required Experience : Five years of hospital operations or patient care experience; two years in accreditation/licensing/regulatory compliance/ quality/performance improvement/patient safety in healthcare; experience applying quality assurance/performance improvement (QAPI) and customer service approaches; experience with Midas, Epic / Electronic Health Record (EHR), County Health Systems, OSHPD.
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Title: regulatory in Oakland, CA
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