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development and execution of control plans Utilize operational performance data to characterize state of control, improvement opportunities and drive process and system optimization Deliver effective business
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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 As a Senior Scientist in the Molecular
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colleagues. Ensures that all regulatory development process commitments are clearly communicated, monitored and met. Acts as the point of contact for all internal Pfizer communication regarding the status
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development process. Collaborates with project teams, subject matter experts, and quality lines to e nsure clear, factual, effective, and appropriately concise presentation of analyses and associated
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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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PHYSICAL/MENTAL REQUIREMENTS Sitting, ability to perform complex data analyses Work Location Assignment:On Premise The annual base salary for this position ranges from $99,900.00 to $166,500.00. In addition
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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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financial resources within the Global Business Unit. Direct a team of colleagues who are responsible for process documentation, training and monitoring of key processes and controls within Business Unit
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Current knowledge of Oncology research, drug discovery and development PHYSICAL/MENTAL REQUIREMENTS Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability
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relevant inbound queries from HCPs via established triage process. In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical (WRD) and Global Product