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of the Oncogenic Transcriptional Networks Group within the Cancer Cell Biology (CCB) Department. The candidate should have expertise in cell line engineering technologies, molecular and protein biology methods, and
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and industry best practices. The Quality and Compliance Lead will also play a key role in driving technology and innovation initiatives to enhance efficiency and effectiveness across the quality and
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Medical Technology or other Health Science related discipline. American Society of Clinical Pathology (ASCP) certified. Minimum of 6 years of relevant work experience in pharmaceutical, hospital, or medical
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timely documentation of experiments in a laboratory notebook Qualifications Must-Have BS degree in biology, chemistry, biochemistry, chemical engineering, or related field with 2-5 years relevant
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others' performance and engagement. Demonstrate clinical and technical skills. Rapidly adopt and utilize new digital technology and other resources with medical customers and record medical interactions
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responses based on how it impacts one's own and others' performance and engagement. Demonstrate clinical and technical skills. Rapidly adopt and utilize new digital technology and other resources with medical
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at country or regional level Responsible for PTA and SIV report review for reports completed by the Site Care Partner Supports implementation of Pfizer's Site Technology Experience systems (e.g. Shared
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for medical professionalism and scientific excellence. By doing all this, we meet our ultimate purpose to ensure that all appropriate patients can safely and effectively benefit from our current and future
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for medical professionalism and scientific excellence. By doing all this, we meet our ultimate purpose to ensure that all appropriate patients can safely and effectively benefit from our current and future