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We are accountable for enabling our programs in early research to reach development candidate nomination through regulatory filing and into clinical trials. How you will Achieve More with Intellia:Intellia is look for a Director, Genotoxicity Regulatory Lead to support the advancement of genome editing products into the clinic.
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Position SummaryThis position is a key leadership role for the development of the In Vivo franchise at CRISPR. Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross-functional teams and partners to bring multiple novel therapies to patients.
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They are seeking a Regulatory Affairs Manager (Contractor) who can provide day-to-day execution for regulatory submissions and compliance requirements. Experience and understanding working with US FDA, European (MDD and MDR), and Global regulatory authorities (ex: Japan PMDA.
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The primary role of the Director, Regulatory Affairs - CMC is to create and/or manage contributions from others for CMC regulatory submission documents. This position reports directly to the Senior Director, Head of Regulatory Affairs - CMC. The Director, Regulatory Affairs - CMC will be responsible and accountable for CMC submission documents while successfully up-holding the vision for the function and help mentoring junior team members.
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10+ years of work experience in pharmaceutical/biotech regulatory affairs, with at least 8 years of Regulatory Operations experience. We are now looking to add capabilities in the Regulatory function and seeking to therefore hire a Director, Regulatory Operations , to join our Regulatory Affairs team and report to our Vice President, Head of Regulatory Affairs & Quality.
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FINRA Brokerage licenses Series 7 & 63 required within 6 months Optimizing the broker dealer clearing/correspondent client experience as it relates to ongoing regulatory reporting obligations Partnering with; Compliance partners to respond to regulatory examinations, including timely and accurate communications to regulator inquiries.
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A career in Treasury Advisory, within Risk & Regulatory Advisory, will allow you to advise financial institutions on developing strategies to optimize financial performance and risk management across financial risks, including liquidity risk, market risk, counterparty credit risk and interest rate risk.
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Requirements: Master's degree in Regulatory Affairs, Engineering, Life Sciences, or closely related technical discipline (willing to accept foreign education equivalent) and five (5) years of experience as a Regulatory Affairs Specialist or experience executing the complete lifecycle of product registrations before national and international regulatory agencies, including documenting internal processes for quality control, and coordinating post-market surveillance and reporting activities.
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This is a newly created role intended for a forward looking, creative regulatory professional able to anticipate and address the challenges involved in swiftly delivering labeling for new respiratory products (COVID, COVID/flu combo and RSV, for example), especially in the United States and other major markets.
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We have an immediate opening for a Financial Regulatory Reporting Analyst in the Financial/Regulatory Reports team. Company Federal Reserve Bank of Boston Financial Regulatory Reporting Analyst Working at the Federal Reserve Bank positions you at the center of the financial world with a unique perspective on national and international markets and economies.
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Firm Type: Law Firm, Experience: 3 Years, A law firm in Boston, MA is seeking a Mid-Level Investment Management Regulatory Associate Attorney with 3-6 years of asset management regulatory experience.
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The EHS Regulatory Compliance Specialist as a resource to the editorial team, while also working in a team environment to maintain, write, edit and post a variety of content and imagery for assigned products.
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About the JobThe Associate Director, Regulatory Affairs works as part of a new product team, focused on improving blood-based cancer diagnostic capabilities in areas such as cancer detection, minimum residual disease, and other related applications.
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Lead a Global Regulatory Strategy Team (GRST) of key contributing members from the regions, emerging markets, RA CMC, Labeling and members of the submission and execution team. The Regulatory Affairs Director (RAD) provides strategic and operational regulatory leadership to the development, commercialization and life cycle management of assigned oncology products.
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Reporting ToVice President, Chief Regulatory Counsel and Primary Security OfficerThe Company Aptiv is a global technology company that develops safe, green, and connected solutions that enable the future of mobility.
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Title: regulatory Company: Flybreeze in Woburn, MA
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