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analysis to build end-to-end solutions and insights that have a direct impact on patient's lives and the future of Pfizer as a data-driven organization. You will be a thought partner to the business
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. Coach colleagues - lead training for routine and non-routine site and process audits. Advise business representatives (e.g. BPOs) on outcomes of complex audits and provides input to process improvement
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in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Job Description Drive GCP quality in documentation, operational data and
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JOB SUMMARY The Medical Writer (Senior Manager/Associate Director) creates documents pertaining to clinical studies and regulatory interactions, including (but not limited to) protocols, clinical
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business representatives ( e.g. BPOs) on outcomes of complex audits and provides input to process improvement activities Independently/with minimal supervision demonstrates leadership by providing clients
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/Business Units, external DM service providers and internal CDS staff to deliver high quality data management for all studies as assigned Proactively drives quality and efficiency to meet timeline and
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/Business Units, external DM service providers and internal CDS staff to deliver high quality data management for all studies as assigned. Proactively drives quality and efficiency to meet timeline and
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support automation computing infrastructure. Provide 24x7x365 support of our automation systems. Responsible for system-wide system compliance, perform business owned system support responsibilities and
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interpersonal and communication skills Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives Proficiency with computer applications (MS Office) Nice-to-Have Master's degree
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ability to achieve work within Early Clinical Sciences. Project management skills preferred. Strong organizational skills and ability to prioritize work a must. Proficiency in MS Office: Word, PowerPoint