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The Regulatory Affairs Specialist supports the oversight of regulatory matters and strategy implementation to ensure the organization complies with applicable regulations. Regulatory Affairs Specialist.
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Assist the Regulatory Affairs Specialist in preparing, submitting, and processing approvals from the IRB and other Penn review entities for new research studies as well as for continuing reviews, modifications, reportable events, and study closures throughout the life of a study.
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The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory queries, and participate in the initiation of the new study, as well as, communicate transition of the new study to the applicable team Regulatory Affairs Specialist post-site initiation.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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Responds to and supports internal and external audit findings as they relate to trade and import and export classifications and accurate government filing. Clients include: Arkema, Dow, DuPont, HARMAN, The Hershey Company, and more.
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Deloitte Risk and Financial Advisory's Financial Services Industry (FSI) Risk, Data and Regulatory professionals help organizations identify the regulatory changes impacting their business and implement effective and efficient processes to manage regulatory, capital, liquidity and interest rate risks, respond to evolving regulatory environments and implement programs, measures, and tools to help clients with a specific focus on risk, data, and regulatory processes.
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Represents Jet Aviation as one company internally and externally with industry groups, regulatory bodies and the General Dynamics network. Represents Jet Aviation as one company internally and externally with industry groups, regulatory bodies and the General Dynamics network.
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Our service offerings include anti-money laundering compliance and investigations; Bribery and corruption investigations; forensic accounting; fraud and other financial crime investigations; governance; risk and regulatory advice; regulatory investigations and litigation support and transactional data analytics.
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Communicate frequently with other Respiratory Sales Specialists across the country and cross-functional counterparts such as Marketing, Sales Ops, Market Access, Field Reimbursement, Training, and Medical Affairs to create alignment of business plan, focus on strategic drivers, and sharing best practices.
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Cal Maritime offers seven baccalaureate degrees in Business Administration, Global Studies and Maritime Affairs, Facilities Engineering Technology, Marine Engineering Technology, Mechanical Engineering, Marine Transportation, and Oceanography.
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Adhere to regulatory standards outlined in the CBH, OMSHA, DPW and Division Manuals. Knowledge and understanding of regulatory standards of care and ability to implement policies and procedures.
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Develop and maintain expertise in a wide range of blockchain technologies, cryptocurrency trends, and regulatory environments. Certification in financial crime investigation (e.g., Certified Fraud Examiner (CFE), Certified Anti-Money Laundering Specialist (CAMS.
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Current experience in Scientific Affairs or Medical Affairs at a biotech or pharmaceutical company. Current experience in Scientific Affairs or Medical Affairs at a biotech or pharmaceutical company.
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Contribute to regulatory responsibilities and obligations, including analyzing existing, proposed, and new regulations and testing of the broker-dealer compliance program. This role focuses on distribution-compliance matters, particularly in marketing material review, broker-dealer regulatory compliance, cross-border distribution compliance, and anti-money laundering (AML.
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Regulatory Compliance: Leads the maintenance of quality assurance standards and requirements for the departmental regulatory aspects of pathology e.g. CMS, DOH, CAP, CLSI, TJC, OSHA, NRC, DEA, FDA and DOT. Maintains database and monitors changes in regulatory requirements from governmental and professional agencies.
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regulatory affairs jobs Title: government affairs in Philadelphia, Columbia, Missouri
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