Principal Biostatistician: Lead Trials with Autonomy

Cytel; Boise (ID); On-site; USD 150,000 - 230,000; Full time

Job summary

Cytel seeks a Principal Biostatistician to lead statistical support for Phase I–IV clinical studies across a client region. You will develop integrated analytical plans, oversee SAPs and ISS/ISEs, and guide cross-functional teams with complex modeling, simulations, and exploratory analyses.

You will collaborate with client teams and Cytel support to ensure regulatory-ready analyses and timely delivery, leveraging R and SAS expertise in a dynamic clinical development environment.

Qualifications

• Master's degree in Statistics or Biostatistics required; PhD preferred.
• 8–10 years biostatistics experience in clinical trials.

Responsibilities

• Lead and influence statistical analyses across trials (Phase I–IV).
• Develop SAPs, ISS/ISE documentation and regulatory submissions.
• Collaborate with cross-functional teams and external vendors.
• Apply advanced modeling, mixed models, and simulations to guide decisions.

Skills

R programming

SAS

CDISC

ISS/ISE

Data visualization

Education

Master's degree in Statistics/Biostatistics

PhD preferred

Tools

Statistical software

Job description

Cytel seeks a Principal Biostatistician to lead statistical support for Phase I–IV clinical studies across a client region. You will develop integrated analytical plans, oversee SAPs and ISS/ISEs, and guide cross-functional teams with complex modeling, simulations, and exploratory analyses.

You will collaborate with client teams and Cytel support to ensure regulatory-ready analyses and timely delivery, leveraging R and SAS expertise in a dynamic clinical development environment.