Senior Principal Biostatistician: Lead Clinical Stats

Incyte Corporation; Wilmington (DE); On-site; USD 120,000 - 180,000; Full time

Job summary

Incyte Corporation in Wilmington, Delaware seeks a senior statistician to lead statistical activities across Phase I–III trials. You will process clinical data for analyses, write SAPs, and contribute to study reports, ensuring high data quality and regulatory compliance.

The role requires a PhD in statistics/biostatistics with pharma experience, SAS proficiency, and collaboration with cross-functional teams and health authorities. On-site presence is expected in a dynamic biopharma environment.

Qualifications

• PhD in Statistics/biostatistics required with pharma/biotech trial experience.
• Strong background in statistical methodology.
• Experience with FDA/EMEA guidelines and drug development.

Responsibilities

• Process clinical data for statistical analysis in trials Phase I-III.
• Lead project teams and coordinate timelines.
• Develop and enforce SOPs and guidelines.
• Write statistical analysis plans and contribute to study reports.
• Interpret results and review statistical summaries.
• Collaborate with multidisciplinary teams and health authorities.

Skills

SAS proficiency

Statistical methodology

Autonomy in project work

Team collaboration

Education

PhD in Statistics/Biostatistics

Tools

SAS

Job description

Incyte Corporation in Wilmington, Delaware seeks a senior statistician to lead statistical activities across Phase I–III trials. You will process clinical data for analyses, write SAPs, and contribute to study reports, ensuring high data quality and regulatory compliance.

The role requires a PhD in statistics/biostatistics with pharma experience, SAS proficiency, and collaboration with cross-functional teams and health authorities. On-site presence is expected in a dynamic biopharma environment.