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Document Preparation: Draft, review, and file legal documents related to trust and estate matters, such as wills, trusts, powers of attorney, advance directives, and probate petitions. The departments are Corporate, Employment Law, Environmental, Family Law, Healthcare, Litigation, Real Estate, Redevelopment & Land Use, Tax, Trusts & Estates.
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Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks and ensuring validity and quality of reported data in the reports, in addition to reviewing DMPK regulatory documents, editing of nonclinical study reports for regulatory acceptance and adherence to company templates, SOPs, DMPK/BA methods, work practices and FDA GLPs, as applicable.
$57.78 - $62.5Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Review/Prepare/Process the Standby Letter of Credit, Commercial Letter of Credit via mail/email/SWIFT and update the Standby Letter of Credit, Commercial Letter of Credit transaction in the Trade Finance system.
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GRA partners with the Lines of Business and Enterprise functions to ensure that its models and analytics address both internal and regulatory requirements, such as quarterly Enterprise Stress Testing (EST), the annual Comprehensive Capital Analysis and Review (CCAR), and the Current Expected Credit Losses (CECL) accounting standard.
$128,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Conduct a brief review of prior FTC agreement service plan, family history in CONNECTIONS and hard case record prior to the FTC.Conduct & participate in debrief meetings prior to FTC and when applicable (a debrief might be required) immediately after an FTC.Ensure debrief meetings occur consistently with Case Planner, Trauma Counselor and/or unit Clinical Supervisor, to consult about any unresolved questions and/or concerns.
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Provide oversight and guidance to CRO for all statistical programming related activities, including development and validation of SDTM and ADaM.•Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician.
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Partnering with the Model Risk Team for request submission for review and approval of use of NLP. The Group's operating companies in the Americas include Sumitomo Mitsui Banking Corp. (SMBC), SMBC Nikko Securities America, Inc., SMBC Capital Markets, Inc., SMBC Rail Services LLC, Manufacturers Bank, JRI America, Inc., SMBC Leasing and Finance, Inc., Banco Sumitomo Mitsui Brasileiro S.A., and Sumitomo Mitsui Finance and Leasing Co., Ltd.
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CAD Drafter Qualifications: Responsibilities: Review Architectural drawings and specifications Prepare shop drawings for Architects approval and fabrication using AutoCAD Prepare B.O.M. Field measure and layout Coordinate details with Architect and General Contractor Draft/Detail Wall Panels/ Curtain wall Trims, Specialty Items such as aluminums screens, Sunshades, Expansion Joints when required.
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The Senior Scientist is responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support initial market applications, post-approval supplements, annual reports, and responses to health authority questions per established business processes and systems.
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Prepare/review technical documents including development/tech transfer reports and CMC regulatory submissions - Participate on cross-functional teams to progress both early and late stage drug candidates.
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). Where permitted by federal or state law, Fidelity will also conduct a pre-employment drug screen, which will review for the following substances: Amphetamines, THC (marijuana), cocaine, opiates, phencyclidine.
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Develops and maintains a compatible and open working relationship with all other departments including at the Brand/Business Division and the M&A team in Hudson Yards, the Operations team, the R&I Métiers, and R&I support groups ( International Ingredient Innovation, Product Safety, Regulatory, Claims, Microbiology, Open Development, and Patents Department) contributing to the Acquisition brands investigation and review.
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Assistant/Associate Professor of Medicine – Infectious Diseases (Medical Director, ID Practice) Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening.
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This is a tenure-eligible, full-time Library Faculty position, requiring a 2nd graduate degree, annual reviews (including a comprehensive third-year review), and service obligations and scholarship for the promotion and tenure process.
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Performs disposition activities for manufactured products in support of clinical products, including MBR, EBR review, and approval and review of CoA. Responsible for Management and maintenance of the Veeva Quality Docs System, including document drafting/Authoring, reviewing, approving, and finalizing internal quality documents (SOPs, Wis, Policies, Forms, etc.
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review job in Elizabeth, NJ
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