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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You
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changing needs of the regulatory environment Works with RQA colleagues on cross GxP audit plans as required Coaches colleagues - leads training for routine and non-routine site and process audits Advises
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and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You
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transparent environment that encourages strong partnerships and mutual trust between teams, sub-teams, and therapeutics areas. Accountable to multiple project/core study teams and clinical sub-teams and manages
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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You
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transparent environment that encourages strong partnerships and mutual trust between teams, sub-teams, and therapeutics areas. Accountable to multiple project/core study teams and clinical sub-teams and manages
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analytical abilities and problem-solving skills. Ability to provide leadership, set priorities and be accountable to timeline . Training in a GCLP/GLP/GMP environment and other international regulatory
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and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
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enhancement opportunities and quality improvements in the different R&D activity areas. Additional responsibilities include ongoing assessment and identification of external environment trends/best practices as