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cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world. What You Will Achieve As an Associate Scientist, you will be
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. You will participate in pre-clinical drug discovery and development
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generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional
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of designated vendors on system support projects and will oversee the development of core communications, SOPs, and/or colleague training materials. Individual project work to meet the team's semester-based goals
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for creating the overarching strategy for early clinical development programs with a focus on innovative design, medical and scientific excellence, and the highest ethical standards. He or she will lead clinical
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ROLE SUMMARY The clinician medical monitor is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design
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ROLE SUMMARY The clinician medical monitor should be able to function independently and have direct experience with all the steps in designing and delivering results of clinical trials by applying
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of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver
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cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world. What You Will Achieve As a Senior Associate Scientist, you will be
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sites/line functions regarding the design, conduct and progression of studies in the PCRU. Assists with the medical and clinical oversight of all aspects of function and work performed within the PCRU