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developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and guidelines. In this role, you will manage and support the operational process and
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therapeutic class, including competitor labeling, to help guide the team in developing labeling text. The GLL provides project management to the Labeling Team throughout the entire process, from the request
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve Resource Operations Associate provides
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training slides and detailed information contained in the site Study Reference Manual. Provide support for queries and resolve issues from global study teams on the sample management process, including
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) 3+ years of management/supervisory experience Experience managing projects PHYSICAL/MENTAL REQUIREMENTS This position/role works in an office where physical requirements are consistent with typical
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assets or CD&O process area and drive learnings across their tumor type(s). Lead Level 1 quality review/assessment during Due Diligence and/or Integration activities. Oversee program and study-level
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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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May manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee pCRO responsible for these activities as applicable Through the Site Care Partner/Country Trial
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve As an Associate Scientist, you will be
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the planning and execution of the Pfizer Oncology Governance document management/review process. The successful candidate serves as a liaison for teams on the Oncology governance process and assists teams in