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stakeholders creating a collaborative network with key internal and external stakeholders. Recommend new approaches to achieve operational effectiveness and efficiency. Identify and communicate situations
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care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and
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, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in
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community of over 50,000 pioneers around the globe. Our teams at Henkel Adhesive Technologies help to transform entire industries and provide our customers with a competitive advantage through adhesives
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This role develops protocols for cross-project consistency and identifying standard case report form modules to meet objectives, as well as communicating key scientific findings to various
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environment with a cross-functional clinical team. BASIC QUALIFICATIONS PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD Strong written and verbal communication skills
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throughout the life cycle. You will participate in a variety of activities, such as, but not limited to, preparing or authoring CMC regulatory investigational, commercial and post-approval submissions
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outcomes and create business impact. NICE-TO-HAVE: Demonstrates stakeholder and conflict management (communications, relationship management) Negotiates needs & acquires feedback on audit outcome Preferred
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provide technical leadership for our systems. Adhere to safe work practices and develop standard operating procedures and system support documentation. Clearly communicate progress and issues to management
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level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards. Provide planning, delivery and communication of statistical analyses, data