As an Associate Director Clinical Pharmacology, this individual is expected to proactively identify and provide significant Pharmacometrics (PMx) contributions, potentially of a complex nature, for research and development programs. They are expected to address strategically important program needs that represent scientific advancements of one or more programs and/or aptly address significant regulatory hurdles. This role is regarded as an expert in the field; as such, the individual is able to contribute to the overall strategic program development and is able to communicate complex PMx strategies and results in an influential manner to the development team. They are also expected to independently design, conduct, and oversee the development of PMx analysis plans and apply standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses.
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Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree