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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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Science, or a discipline relevant to clinical trials, or PharmD. At least 10 years' experience in clinical research and 5 or more years' experience in the pharmaceutical industry or related organizations
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and applicable internal, external, regulatory requirements. Quality Oversight for study types conducted in the real world evidence generation platform including Non-Interventional, Low Interventional
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. Experience collaborating with academic medical centers and other healthcare partners. Sound understanding of electronic health records systems and principles of data quality for real-world data. Strong ability
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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critical review and management of proposed and ongoing global investigator-sponsored research studies. Assist in partnership with RWE colleagues to analyze and publish real-world data studies as needed
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Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and
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value of Pfizer medicines to inform patient access more fully to medication decision-making and improve population health through communication of real-world data analyses, pharmacoeconomic analyses