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and be accountable for effective study team operations Accountable for issue escalation and resolution Lead study team chartering and team health check process Governance & Decision Points Drive
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colleagues, complete review and witnessing of all experiments. Summarize and document results in process safety test reports Lead technology development and workflow initiatives to implement new capabilities
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-class process safety capabilities. Responsible for maintaining lab facilities in a neat and orderly manner complying with all local safety practices. In conjunction with the Groton, CT process safety lead
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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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Clinical Research and may take the lead on company-wide, global process improvement initiatives, and champion's process enhancements and solutions for complex issues. Leads change for Vaccine Clinical
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sub team(s) to ensure collaboration and seamless connectivity. ROLE RESPONSIBILITIES Responsibility to assist/lead development and execution of simple to moderately complex clinical studies; on more
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into brand strategies and tactics, aligning on US regional medical needs, across different assets and maintaining consistency across different products according to the US Thoracic Oncology strategy Lead the
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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 In this role, you will be joining a
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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 Designing new medicines at Pfizer
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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. Role Summary We are looking for an Automation Engineer who will