Associate Principal Statistical Analyst

10-14 years of Statistical Programming experience in biotechnology or pharmaceutical industry.

Direct statistical programming experience for early or late-phase clinical trials to support production/verification of analysis datasets, tables, listings, and figures.

Early or late-stage oncology clinical trials.

Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment.

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Position requires about 10-14 years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early or late phase) within Statistical Programming function.

In addition to direct programming and technical oversight of one or more studies, this position may require assistance providing technical support and guidance during regulatory submissions while ensuring conformance to CDISC standards and submission guidelines.

Based on company needs, this position may be required to lead an early Phase or late phase study or program.

Provide technical oversight of statistical programming resources including contractors and CROs.

Provide mentorship to future leaders to help learn and execute on RevMed core values.

Ensure quality and timely delivery of analysis for statistical programming deliverables.