Contribute to design, analysis and reporting of clinical trials or other scientific research
Assist with development of protocols and/or statistical analysis plans.
Assist in identifying scientifically appropriate data collection instruments.
With supervision perform statistical analyses as per the analysis plan.
Collaborate with Statistical Programming to ensure the delivery of high-quality outputs.
Develop strategy for data presentation and inference.

🎯 Requirements

MS (with 4+ years of experience) or PhD in Statistics, Biostatistics, or a highly related field.
Experience with R and SAS
Experience with statistical computations and simulations

🎁 Benefits

Paid time off (vacation, holidays, sick)
Medical/dental/vision insurance
401(k) to eligible employees
Short-term incentive programs

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