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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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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 This is a laboratory-based position within
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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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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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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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. • Responsible for proactive risk management and inspection readiness for their clinical study(ies). Your responsibilities may also include: • Ensures comprehensive operational input to submission plan. • Lead the
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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