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10+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs / small molecules.
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Global Regulatory Policy Manager – Liquidity covers a number of key aspects of prudential interpretation, including risk weighted assets (RWAs), capital resources, and the leverage ratio, across a full range of risk areas e.g. credit risk, counterparty credit risk, liquidity risk, securitisation, market risk, etc.
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BODYARMOR is looking for a Senior Regulatory and Supplier Quality Manager! The S enior Regulatory and Supplier Quality Manager develops, improves, and drives compliance to all Regulatory and Supplier Quality requirements at BODYARMOR. This person will be a strong leader who works well cross functionally to assure Regulations in the country of sale are applied and complied to at the design phase of Innovation through to first production and in-market.
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The IRB Regulatory Consultant will oversee regulatory operations of studies conducted by one or more Disease and Modality Team within Montefiore Einstein Cancer Center, including, internal (investigator-initiated studies), Cooperative group, and industrial protocols (pharmaceutical and biotechnology company studies.
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Accreditation and Regulatory Specialist | Luminis Health. Minimum three years of experience in accreditation and regulatory compliance or Quality Management. Serve as the expert resource on regulatory/accreditation and licensure standards.
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We’re seeking a future team member for the role of Capital Markets Broker Dealer Regulatory Reporting Analyst to join our Capital Markets Accounting team. Capital Markets Broker Dealer Regulatory Reporting AnalystBring your ideas.
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Develop, document, and lead the implementation of the BODYARMOR Regulatory requirements through policy and procedure. Lead and drive compliance to the BODYARMOR Regulatory program end to end.
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The Associate Principal Scientist is responsible for developing and implementing Regulatory CMC strategies for assigned small molecule products in accordance with global regulations and guidance's, and Company procedures.
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Consultant, Regulatory Specialist, Tissue Bank/Pharmaceutical. Regulatory Affairs Certification (RAC) or Certified Tissue Bank Specialist (CTBS) certification preferred. Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist.
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Execute regulatory strategies by leading the development, authoring, and review of CMC submission components and documentation to support post-approval supplements, annual reports, registration renewals, and responses to health authority questions per established business processes and systems.
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The Global Markets Regulatory Compliance (GMRC) Advisory Vice President is responsible for providing advice on Swap Dealer and Broker Dealer regulations (including the global impact of relevant U.S. regulations) and internal policies and procedures to internal stakeholders, including trading and sales personnel and key support functions.
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Regulatory Operations team is responsible for reporting to external stakeholders in the North America region, including the reporting and monitoring of trade, transaction and position information across a wide range of traded financial products and business lines for the CFTC (Commodity Futures Trading Commission), SEC (Securities and Exchange Commission), and CSA (Canadian Standards Association) obligations.
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Join Takeda as a Director, Precision Medicine and Digital Health where you will be responsible for providing strategic guidance and oversight for the delivery of global regulatory strategies to support the development of biomarkers, diagnostic tests, devices, and digital health tools to enhance the value of our products across therapeutic areas.
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We are seeking a highly motivated and experienced Associate Director Regulatory Affairs with expertise in hematology / oncology to join our Drug Discovery and Early Development team. Experience managing regulatory affairs in Hematology/Oncology is required.
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Experience with CMC regulatory documents (global registrations, including NDAs, MAAs and others, responses and supplements/variations) Participating in the development of the CMC regulatory strategy for post-approval small molecule product submissions, including global supplements/variations and responses to health authority queries.
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Title: regulatory Company: Clarivate Plc in Bronx, NY
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