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of the discipline will make you a critical member of the team. You are proactive in contributing to all team discussions and creating an environment of collaboration. It is your hard work and focus that will help in
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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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a remote environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent judgment skills and work in a continuous improvement environment. Work within a
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handle feedback and conflict constructively. Demonstrate ability to manage a significant volume of projects developed in a remote environment, while exhibiting the ability to prioritize, successfully
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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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of assigned customers. Lead and/or manage a significant volume of projects developed in a field-based environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent
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OR ENVIRONMENT REQUIREMENTS This position involves a non-standard work schedule, working Sunday through Thursday. A scheduled workday would consist of a total of 8 hours, between 10:00 a.m. and 9:00 p.m
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generation RNA therapeutics design and drug discovery Proficiency with deep learning frameworks and data structures Excellent organizational skills, with ability to navigate a complex matrix environment and
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and/or characterize biomolecules PHYSICAL/MENTAL REQUIREMENTS Standard laboratory conditions - sitting & standing for periods of time NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS 40