Provide statistical support to R&D, including clinical trials and patient safety.
Collaborate with cross-functional teams to design, analyze, and report trials.
Prepare protocols and analysis plans with programming details for implementation.
Report data issues and ensure high-quality statistical outputs on timelines.
Interpret statistical results and support publications and presentations.

🎯 Requirements

MS or PhD in Statistics, Biostatistics, or related field.
4+ years performing statistical computations and simulations.
Experience in oncology and pharma clinical trials preferred.
Strong communication skills and ability to collaborate cross-functionally.

🎁 Benefits

Competitive compensation package and comprehensive benefits.
Eligibility for short-term incentive programs.

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