Biostatistician I

Statistics Interest Group; Northern (KY); Hybrid; USD 100,000 - 150,000; Full time

Job summary

Medpace seeks a Ph.D. in Biostatistics or Statistics to contribute to clinical development, plan preparation, and statistical methodologies. You will review study protocols and perform SAS-based analyses for complex clinical data.

Responsibilities include programming study analyses, preparing methods sections for reports, and communicating requirements for CRF design, database design, and data cleanup, ensuring key variables are analysis-ready; and communicating results to medical writing.

Qualifications

• Ph.D. degree in Biostatistics / Statistics with strong SAS programming experience.
• 1–2 years of experience in a pharmaceutical or CRO setting preferred.

Responsibilities

• Contribute to clinical development of plan preparation;
• Review of study protocol and preparation of statistical methodologies;
• Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;
• Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and
• Communicate statistical results to medical writing personnel to ensure accurate interpretation

Skills

SAS Programming

Biostatistics

Education

Ph.D. in Biostatistics / Statistics

Job description

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Company Name Medpace

Company Information

Duties and Responsibilities

Contribute to clinical development of plan preparation;

Review of study protocol and preparation of statistical methodologies;

Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;

Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and

Communicate statistical results to medical writing personnel to ensure accurate interpretation

Position Qualifications

Ph.D. degree in Biostatistics / Statistics with strong experience in SAS Programming or equivalent; and

1-2 years of experience in a pharmaceutical or CRO setting preferred