Contribute to design, analysis and reporting of clinical trials or other scientific research
Assist with development of protocols and/or statistical analysis plans with details for programming
Work under supervision to implement sound statistical methodology in scientific investigations.
Assist in identifying scientifically appropriate data collection instruments.
Identify and report data issues or violations of study assumptions.
Provide programming specifications for derived variables and analysis datasets.

🎯 Requirements

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

🎁 Benefits

Comprehensive package of benefits including paid time off (vacation, holidays, sick)
Eligible to participate in our short-term incentive programs.

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