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Minimum 7 years of knowledge of Third-Party Risk Management methodologies and regulatory guidance and or risk management at a fintech organization. Well versed in financial regulatory and supervisory expectations in the risk areas.
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O Facilitate the implementation of CAPA for non-conformances and root cause evaluation from internal and external audits, regulatory audits, environmental monitoring, and cleaning validation methods such as ATP and allergen validation.
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Use geospatial data analytics, related software (ArcGIS or similar), calculations and models to address impact, regulatory and climate change issues. Assist in the data collection, analysis, reporting and client engagement to assess a wide variety of physical, regulatory, and reputational water stress factors and their business risk impacts.
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The base salary range for the Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology is from :181,000-237,600. This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communication materials.
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Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings. Associate Scientist / Bioanalytical Services Essential Functions Provide support for running sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment.
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Deep knowledge of products, working knowledge of the regulatory environment, and of local insurance and surety markets. Bond & Specialty Insurance provides management and professional liability insurance, as well as surety bonds to businesses and non-profit organizations of all sizes.
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The Sr Director, Regulatory Affairs CMC is responsible for identifying and evaluating CMC issues associated with product development including product and process development, device development, analytical methods, formulation development, manufacturing, and labeling.
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Job Snap Shot: Under the general supervision of the Executive Director, the Human Resource Generalist provides comprehensive administrative support across HR functional areas including recruitment and onboarding, payroll processing, employee records maintenance, benefits and leave of absence administration, performance management administration, regulatory compliance, offboarding and unemployment compensation administration.
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Serve as a SME for the SEC's Liquidity Rule (Rule 22e-4) and Derivatives Rule (Rule 18f-4) Support regulatory compliance by completing monthly liquidity reviews to ensure security classifications are current and resolving potential liquidity breaches as needed.
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Work cross-functionally to bring appropriate analogues/historical knowledge to project impact of promotional efforts, market access changes, competitive events, scientific developments, regulatory evolution, etc.
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The Office of Educational Accessibility (OEA) is a member of the Academic Affairs Division. Terminal degree in higher education, student affairs, disability studies, counseling, law (Civil Right or Education Law), or other related discipline; and/or.
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Tour the facility at regular intervals to check building security and ensure there are no fire or safety hazards in accordance with program and regulatory policies. With your help, we can turn the tide on substance use disorder.
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Ensure property maintenance related to inclement weather, including shoveling, salting, and de-icing walkways and vehicles, as directed. Those interested in applying for this role should be willing to work at least one evening shift per week, and a rotating weekend shift as needed (if working in a residential environment.
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The Oncology Infusion Pharmacist is responsible for overseeing both hazardous and non-hazardous sterile compounding and ensuring compliance with regulatory requirements. The Oncology Infusion Pharmacist is responsible for overseeing both hazardous and non-hazardous sterile compounding and ensuring compliance with regulatory requirements.
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The Contract Quality Systems Manager will ensure on-going compliance to applicable compendia, GMP’s, and Regulatory guidance. Develop and manage processes that ensure the Exton site remains in compliance with global quality polices, regulatory requirements, and industry requirements, including periodic review and consolidation.
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regulatory affairs jobs Company: Vector Marketing in West Chester, PA
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