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The Senior Clinical Research Coordinator will complete all study related procedures and distribute study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director.
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In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.
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Clinical Research Coordinator B: In addition to the above, the CRC B will establish workflows, pathways, and methods to operationalize protocols, regularly prepare, draft, and submit regulatory correspondences, and mentor/train less experienced research staff in the completion of their duties when required.
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QPS, LLC has an opening for a Research Scientist in the Bioanalytical unit of QPS’ Distribution, Metabolism, Pharmacokinetics (DMPK) department. Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services.
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Essential Functions: Supports well-defined research with minimal supervision from the DOR Research Scientist I, II or III. Prepares draft grant proposals, internal reports and publications independently and collaboratively for review by Senior Scientist.
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Review documents and draft responses to records and subpoena requests, including Public Information Act (PIA) or FOIA requests as needed. Conduct research, including legal research and research of e-filings/docket filings.
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The Deputy General Counsel will draft, negotiate and complete real estate transactions, represent OCII in various proceedings, conduct research and interpret statutes, draft legal documents and opinions, and advise OCII commissioners and staff.
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In particular, the PC will draft and negotiate agreements related to data collection and use, research and & analytics, distribution of advertising inventory on non-Disney controlled platforms, advertising technology, linear addressable and data driven linear services, programmatic advertising, insertion orders, master terms and conditions with advertisers and agencies, integrated marketing, branded and custom content, influencer marketing, and social media platforms.
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Assist In-House Counsel with special legal projects / legal research / legal correspondence as assigned. Draft, review and redline SNDAs, Estoppel Certificates, and Lease Memorandums. Review and draft LOIs.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Reviews and conducts research for ROI (Release of Information) Reviews new cases and conducts research of pertinent laws Edits previously submitted final decisions and writes/researches legal opinions on newest case Edits and reviews cases for issuance Responds to citizen letters Reviews AMICUS briefs Briefs attorneys regarding legal issues, theories and draft statement of facts.
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Conceptualize, draft, and edit external editorial materials including op/eds, letters-to-editor, blog posts, social media posts, email correspondence and letters, and video scripts for CEO and other senior executives.
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Draft, negotiate and review market access related agreements, including: PBM agreements, GPO agreements, Specialty Pharmacy agreements, wholesaler agreements, discount and rebate agreements, distribution agreements, innovative/value-based agreements, market research agreements, vendor agreements, and service agreements.
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Structure, draft, and negotiate contracts relating to data collection and use, research and & analytics, distribution of advertising inventory on non-Disney controlled platforms, advertising technology, linear addressable and data driven linear services, programmatic advertising, insertion orders, master terms and conditions with advertisers and agencies, integrated marketing, branded and custom content, influencer marketing, and social media platforms.
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Draft/revise SOPs and work instructions for sample management activities. Title : Research Associate. Knowledge of general lab assays is required (e.g., Cell culture, ELISA, Flow Cytometry, Molecular Biology), but experience is preferred.
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