Principal Biostatistician Consultant at ClinChoice overseeing drug development statistical methodologies. Lead statistician for clinical studies in a hybrid work environment.
Responsibilities
Work with Biometrics director to manage one or more compounds/Indications in R&D for the entire life cycle.
Responsible for all statistical aspects of the drug development and/or post-approval programs.
Coordinate statistical and programming support and manage contractors/CROs when necessary.
Serve as lead statistician for clinical studies and collaborate effectively with the study team members.
Requirements
M.S. or Ph.D. (or equivalent) in Statistics or Biostatistics is required.
Minimum 4 years (Ph.D.) or 8 years (M.S.) pharmaceutical industry experience
Should possess experience interacting with regulatory agencies (e.g. FDA, MHRA or EMEA).
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