Contribute to design of early/late-stage protocols across multiple therapeutic areas.
Draft protocols or amendments; develop and write Statistical Analysis Plans.
Perform statistical analyses for interim and final regulatory reports.
Support submissions; design/analysis/report integrated safety/efficacy summaries.
Attend study team meetings and contribute to leadership within the BDM Department.

🎯 Requirements

MS or PhD in Statistics or Biostatistics
PhD +4 years (or MS +9 years) in biotech/pharma clinical trials
Hands-on Phase I/II/III clinical trials; SAS programming; R desirable.
Excellent oral and written communication skills.
Experience with regulatory submissions in US, Europe, Japan, RoW desirable.

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