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formulation and characterization Proficiency in High-Content Imaging using confocal microscopies and associated imaging software Proficiency in process development of mRNA-LNP & automation solutions NON
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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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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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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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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY You will represent Biostatistics on cross
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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
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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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set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
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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