Collaborate with study teams to design early/late-stage protocols.
Draft protocols/amendments and develop statistical analysis plans.
Perform statistical analyses for interim and final regulatory reports.
Support submission activities including integrated safety and efficacy summaries.
Attend study team meetings with statisticians and data managers.

🎯 Requirements

MS or PhD in Statistics or Biostatistics
PhD +4 years (or MS +9 years) clinical trial experience
Hands-on Phase I/II/III clinical trials; SAS programming; R desirable.
Excellent oral and written communication skills.
Regulatory submissions experience desirable.
Exposure to regulatory submissions in US, Europe, Japan is desirable.

🎁 Benefits

Equal opportunity employer; inclusive hiring practices.
Remote work option in Canada.
Career development and professional growth opportunities.

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