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Document and communicate on a daily basis all facets of the day shift operation to the Assistant Program Director and Program Director, including the implementation of the Standards of Care legislation and Shelter Grievance Policy.
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You will report to the Sr Director, FP&A PDMS, who is a member of the Autodesk Financial Planning & Analysis organization. Manage policy exceptions and document approvalsSubmit and secure export control checks to the Global Trade Compliance teamInvoice customers/partners and manage accounts receivable collectionsFulfill orders by providing customers access to purchased softwareUpload transaction support to central repositoryProvide revenue accounting with month-end close package for revenue recognition.
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Working with Director of Finance and Chief Financial Officer (CFO) to manage seasonal borrowing. Manage accounting specialists and firm uploads of Lexis/Nexis, Document Processing, Litigation and E-Discovery, Patent Fixed Fees, USPTO charges.
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Reporting to the our CMC Executive Director, the CMC Regulatory Technical Writer, Associate Director/Director will be responsible for CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all CMC technical writing objectives are met.
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We're looking for an experienced Associate Creative Director/Writer on the Aquent Studios x Adobe team who will support always-on and seasonal campaign creative with a focus on Acrobat and Document Cloud.
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As an Aquent Studio team member, you'll have the opportunity to engage with the largest and most influential companies in the world, solving design challenges and extending their brands across tactic types and platforms, including digital design, UI/UX, video, motion, content, print design, web development, and more.
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Must also be aware of the rehabilitative and preventative aspects concerning each resident, their safety, comfort, and protection, the usual performances indicated for disease prevention and restorative measures, the ability to document professional nursing services provided with a realistic plan for reaching short and long term goals, and to be able to make decisions regarding safety needs of residents including adequate equipment.
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The Associate Director, Clinical Records & Information Management will partner with cross functional teams as well as Clinical Research Organization (CRO and Functional Service Provider (FSP) to ensure timely and quality delivery of the TMF. This role is a member of the Clinical Records leadership team to ensure optimum implementation of the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program.
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Ensure compliance with applicable health authority regulations and guidelines for document management, TMF, and software used in GCP processes. Reporting to the Vice President of Quality, the Senior/Executive Director of GCP Clinical Quality Assurance is responsible for partnering with Clinical Operations to ensure that quality and compliance are integrated into long term strategies and day to day operations.
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Collaborate with grade level partner(s), Director of Arts Programming, Arts Specialists, and/or visiting artists to develop and document arts-integrated curriculum and instruction, as well as evaluate and assess current curricular models and practices and make student learning visible.
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Leads statistical analysis, document review and data inclusion for NDA submissions of assigned studies by collaborating with other Biostatistics team members and cross-functional partners. With increasing independence, you will lead biostatistical analysis and reporting, document review and data inclusion for NDA submissions of assigned studies by collaborating with cross-functional partners to meet clinical development project deliverables and timelines.
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Experience with cloud-based document management programs (e.g., Veeva) and/or document management systems and co-authoring tools. The Associate Director, Regulatory Affairs is part of the Alector Regulatory Affairs team based in the San Francisco Bay Area. This individual will support regulatory activities critical to the company’s product development objectives as regional and regulatory support for one or more programs and leads cross-functional initiatives.
$200,000 - $228,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Tenant Improvement/Special Projects Director of Preconstruction. Understand the full scope of the project through document review and asking questions of the design team and owner. The Chief Estimator is responsible for all aspects of estimating the most complex Tenant Improvement (Retail, Restaurant, Office, Hospitality) and Special Projects (Seismic, Public Work, Healthcare, Life Science, Institutional)including pre-construction, hard bids, negotiated bids, budgets, general conditions, systems studies and comparisons, value engineering, subcontractor relations and staying abreast of industry developments applicable to estimating.
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The lowest commission earned by an Area Director in the top 10% of payments was $117,967. The average commission for the top 10% of Area Director franchisees with one Stroll publication is $149,000.
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HR ProjectsAssist the Bay Area HR Team with a variety of human resources projects, including, but not limited to document audits, file digitization, summer internship coordination, and community outreach programming.
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director document jobs in South San Francisco, CA
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