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results Presentation of results within a multidisciplinary team environment. Ensure appropriate use of animals in compliance with all regulatory requirements and internal standards. BASIC QUALIFICATIONS
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development, knowledge of publication processes, data generation activities, medical communications, regulatory, clinical and pharmacovigilance environment in International IDM. Knowledge of the key
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) Understanding of clinical development, knowledge of publication processes, data generation activities, medical communications, regulatory, clinical and pharmacovigilance environment in International IDM
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environment on several research programs simultaneously with aggressive timelines. Able to work with limited daily supervision. Nice-to-Have Hands-on experience in flow cytometry Drug discovery experience
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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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of applying knowledge of principles, concepts, and practices 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
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internal company leadership and colleagues, as well as external collaborators, including investigators/medical professionals Is a team player, works well in a team environment both as a leader and a key
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for results and generate innovative solutions with minimum supervision. Applicants should be self-motivated, organized, capable of working independently, and in a collaborative environment. The successful
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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 global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate