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withstanding regulatory scrutiny. This position will focus primarily in Trial Master File Operations. Facilitate the execution of the TMF Operations' activities to enable complete, compliant and consistent study
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POSITION SUMMARY You will join a team of scientists supporting oncology development programs. You will be the primary Clinical Pharmacology Lead providing clinical pharmacology expertise to a
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required in an analytical type function, which can include: consulting, primary quantitative market research, secondary data analysis, forecasting, predictive modeling. Understanding of the specialty
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recommendations Demonstrated ability to manage vendors to ensure effective project delivery Nice-to-Have Master's degree Experience in quality control and/or quality assurance within the pharmaceutical industry