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Associate Principal Scientist
Develops, coordinates, and provides leadership for the development and implementation of open-source software projects in clinical trial design and analysis.
Collaborates on and/or leads statistical research for clinical trial design and analysis.
Is aware of and collaborates on evolving standards in open-source software in the regulated pharmaceutical development environment.
Consults with clinical trial teams to implement advanced design and analysis.
Interacts with contractors on significant outsourcing projects.
Collaborates on internal standards development and training.
Ph.D. or equivalent degree in statistics/biostatistics/computer science/data science or related quantitative discipline with a minimum of 3 years of relevant work experience, or a Master’s degree with a minimum of 6 years of relevant work experience.