Independently contribute to design of early/late-stage protocols across multiple therapeutic areas.
Draft protocols or amendments and develop/write statistical analysis plans.
Perform statistical analyses for interim and final regulatory reports.
Support submission activities and integrated safety/efficacy summaries.
Represent Biostatistics in client/project team discussions.

🎯 Requirements

MS or PhD in Statistics or Biostatistics.
PhD + 6 years or MS + 11 years clinical trial experience.
Hands-on Phase I–III clinical trial experience; SAS; R desirable.
Excellent oral and written communication skills.
Regulatory submissions experience in US/Europe/Japan desirable.

🎁 Benefits

Equal opportunity employer; values diversity.
Inclusive, barrier-free recruitment; accommodations on request.
Client-facing, collaborative culture with strong development.

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