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to support decision making in the drug development process. The General Toxicology R6 Study Director is responsible for the design, conduct, interpretation, and reporting of exploratory, mechanistic and GLP in
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strategic regulatory expertise as Global regulatory representative to Product Team(s). As a Director, Lead and coordinate a virtual global regulatory strategy team (GRST), encompassing regional regulatory
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As a member of a team of scientists in our In Vivo Pharmacology Cancer Cell Biology Group, you will play a lead role in using models of cancer to evaluate new drug candidates, mechanisms, and
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practices for partnered programs. You will ensure creation of strategic and operational objectives from early (lead) development through Proof of Concept and licensure of the product depending on the program
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. We are looking for a Sr.Director / Team Leader, Data Science and AI who will be responsible for building and scaling AI-powered analytic tools to Pfizer's Commercial organization and lead a team of ~5
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Compliance Lead with a focus on GMP principals across our Global Materials Management group. The successful candidate will ensure the highest level of quality and compliance across all aspects of GMM
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Compliance policies and Regulatory requirements and enables monitoring of processes and standards. Lead the identification and initiation of continuous process improvements to enhance the quality of operations
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ROLE SUMMARY: Lead as a player/coach the group of Asset Quality Leaders and accountable for the management and oversight of GCP performance and quality systems within the oncology portfolio
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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 The ADC Chemistry (AC) group is seeking a
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regulations Independently conducts wide range of routine/(non-routine) complex investigator site audits (minimal to no oversight - as needed) Executes audit strategy, leads/supports process audits, and may