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With a high degree of visibility and coordination with Finance and Compliance Leadership, the Financial Reporting Senior Accountant is responsible for supporting GAAP financial reporting, regulatory reporting, and covenant reporting for a national mortgage bank and wholly owned subsidiary of a publicly traded company.
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Oversee the Tax Accounting functions, including regulatory reporting with government agencies (sales / use tax), represent Express on tax audits with outside government agencies (sales / use tax audits), facilitate communication with appropriate government agencies and company counsel related to tax matters, formulate tax projections for quarterly income tax payments, for preparation for city, states and federal tax returns with outside public accounting firm (Grant Thornton.
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Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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Public Safety Officers provide support to many areas of the University including Student Affairs, Facilities, Academic Affairs and Athletics. Knowledge of dispatch systems, radio communications, fire systems, CCTV, emergency procedures and switchboard communications is a plus.
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We are looking for a Senior Environmental Project Manager with strong contaminant hydrogeology technical skills, strong working knowledge and experience withthe PA environmental regulatory programs, specifically Act 2, Registered Professional Geologist in PA and a collaborative working style to join our team in the Philadelphia, PA region.
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Experience in drug development, including writing of DMPK contributions to regulatory documents (e.g., IND/CTA/IB etc) would be preferred. Have comprehensive knowledge of relevant pharmacokinetics (PK) principles, and experience integrating PK/ADME data with pharmacology and toxicology profiles.
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Support/lead other Medical Affairs activities including: medical information, medical education & grants, HEOR/RWE and medical operations. Works closely with the MSLs to ensure strategic intent meets tactical implementation (seamless transition between upstream and downstream medical affairs.
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About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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Interface with External Affairs and Alumni Relations and various SCS offices pertaining to events, meetings, and guests' reservations. Interface with External Affairs and Alumni Relations and various SCS offices pertaining to events, meetings, and guests' reservations.
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Participate in the preparation, assembly and filing of CMC regulatory submissions to support development stage and new product approvals, including interactions between the company and health authority representatives to facilitate submissions.
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Comprehensive understanding of applicable standards, methods, processes and practices, business fundamentals, and performance metrics in the specific functional area supported by this position (e.g., asset management, electric or gas operations, customer service, transmission and substation, distribution system operations, regulatory and external affairs, transmission operations and planning.
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Works in compliance with all regulatory standards including EH&S, cGMP, Radiation Safety, applicable pharmacy laws, DOT, and internal policies and interpretations of the above as required.
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The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates and may have direct interactions with health technology assessment (HTA) agencies, reimbursement decision makers and national immunization technical advisory groups.
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Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion. This Sr. Clinical Research Coordinator opportunity will be patient facing and will provide support with samples and sample processing.
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In compliance with SOPs and GLP regulations. Perform laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs) study protocols, study and laboratory-specific methods or procedures, and company policies/practices.
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regulatory affairs jobs Title: compliance Company: Kroll in Horsham, PA
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