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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 Clinical Research will be responsible for thehase 2, PoM and SoCA trial designs and implementation of the study in collaboration with Pfizer development operations and the project team to meet
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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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' scientific and technical developments in preclinical to clinical translation and apply these where possible to advance the portfolio programs . Conceptualize and design experiments . Mentor junior scientists
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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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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 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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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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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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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