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therefore expected that the candidate will have deep expertise in computational and data science methods, but also be able to bridge that knowledge to fundamental questions of biology and clinical impact
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to microbiological techniques acquired in academic/industrial setting. 2. Strong communication and computer/technical skills. \nRelocation support available\n Work Location Assignment: On Premise The annual base
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ROLE SUMMARY This position is for a Medical Director within the Tisotumab Vedotin program. This position will be responsible for supporting a late-stage clinical trial. The successful candidate
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Engineering or related Mechatronics discipline (or within 6 months of completing a program) or an B.S. with 3+ years' experience in a related field. No industrial experience necessary. Experience with robotic
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experimentation through enhanced analytics, computer vision and other emerging technologies. Develop and implement synergistic digital tools for machine learning and self-optimization to enhance automation goals
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for participation in Pfizer's Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous
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quality and population health. Maintain, continually develop, and utilize clinical informatics capabilities to enable effective collaborations with external customers. Facilitate development of clinical
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team of an oncology program. ROLE RESPONSIBILITIES Acts as Clinical Pharmacology representative on Clinical Sub Team and Development Team, as appropriate. Provides the clinical pharmacology components
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regulated operations. The Senior Manager Auditor , is responsible for the delivery and execution of the global Quality Assurance (QA) program audit activities on assigned GxP enterprise processes that span
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analysis for multiple analyses supporting a program. Prepare formal presentations and written reports to Pfizer standards. Contribute to regulatory documents (summary documents, briefing books, regulatory