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Manages responses to requests involving Securities and Exchange Commission (SEC) oversight inspections and examinations, which includes the identification and collection of responsive documents, conducting due diligence reviews on proposed responses, drafting response letters, obtaining necessary supervisory approvals, and coordinating with other Regulatory Operations (RegOps) groups and FINRA’s Office of Oversight Liaison and Counsel (OLC) to make timely and accurate productions.
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Center 2 (19050), United States of America, McLean, VirginiaSenior Associate - AccountingAs a key component of resiliency, Liquidity in a post-COVID environment has been a key focus area for financial markets and Regulatory Agencies.
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Applicable code of state regulations for adult and children services and local regulatory operations. Trauma-informed care and positive behavior support. Applicable code of state regulations for adult and children services and local regulatory operations.
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Ensures loan originations are in accordance with regulatory compliance. Ensures documentation is completed in accordance with regulatory compliance. Sponsorship Statement As a condition of employment, individuals must be authorized to work in the United States without sponsorship for a work visa by Fulton Bank currently or in the future.
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As a Mobile Associate, you will be required to successfully complete new employee training. At T-Mobile, we strongly encourage everyone, including people of color, veterans, military spouses, individuals with disabilities, lesbian, gay, bisexual, transgender, queer and non-binary people, and parents to apply.
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Familiar with current regulatory guidance and industry best practices for development and validation of bioanalytical methods for large molecule biologics. Experience in GLP and/or clinical regulatory compliance.
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A minimum of 10 years of experience in Regulatory Affairs, CMC Biologics (Bachelor's degree requires at least 12 years) Work with VP of Regulatory Affairs to identify resource needs, including consultants and new associates, advising on skills sets to meet needs.
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Biotechnology, Pharmaceuticals, Healthcare, Clinical Research, Chemicals, Laboratory Services, Research and Development, Regulatory Affairs, Science and Research, Laboratory Testing. Senior Financial Analyst for USAID-funded Global Health Projects.
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Utilize resources available for safety and regulatory standards (IEEE, IEC, NEC, NESC, NERC, ISO/RTO) to effectively define project requirements, review project deliverables (physical, P&C, power system design) and collaborate with owner and OEM resources (subject matter experts, internal engineering, and project management.
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The Quality/Regulatory Compliance Director provides leadership and evaluation of all organizational quality and performance improvement activities and regulatory requirements for all applicable regulatory bodies.
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HJF is seeking a Regulatory Affairs Coordinator to be responsible for assisting in the compliance of HJF research programs with applicable local, state and federal regulations for human subjects research, animal use research, recombinant DNA, and Health Insurance Portability and Accountability Act (HIPAA.
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Collaborate with clients, regulatory agencies, and internal teams, including VIKA’s Engineering, Landscape Architecture, Surveying, and Planning Staff, as well as external consultants, to facilitate project coordination and communication.
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Oversee the School’s accounting and reporting functions, including all earned revenue payments and collection, accounts payable, contracting, payroll, grants management and reporting, regulatory reporting and compliance, and other business administration activities.
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The Office of the General Counsel’s (OGC) Legal Internship provides law students with an opportunity to build valuable legal and professional skills in research, writing, and advocacy, while learning about different areas of OGC’s work, such as civil litigation, regulatory matters, employment law, privacy law, contracts, and more.
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Keeps abreast of and ensures compliance with regulatory practices (e.g. FDA, EMA, and ICH guidance and recommendations) and industry data standards (e.g. CDISC). Represents Emmes at Sponsor, Regulatory, Investigator or Safety Review meetings (e.g., Data and Safety Monitoring Board Meetings.
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regulatory affairs jobs Title: sr regulatory affairs associate in Rockville, MD
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