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In this role, one will work closely with clinical pharmacometricians, physicians, and other scientists, applying your expertise and leadership skills to contribute to the strategy of the clinical program. One will influence key decisions in early and late phases of clinical development, ensuring expert data integration, analysis, interpretation, and reporting of clinical pharmacology results.
As a Senior Director, you will be responsible for developing a culture supportive of MIDD approaches within the TA, planning and executing state-of-the-art modeling and simulation (M&S) techniques, providing scientific and strategic input into pre-clinical, clinical, and post-approval development plans, and much more.