Senior/Principal Statistician Consultant --TA - Oncology (Remote)

ClinChoice

1d • Remote

About The Position

ClinChoice is seeking a Senior/Principal Statistician Consultant to provide statistical expertise and operational support for oncology clinical trial projects across a diverse client portfolio. The contractor will help ensure the accuracy, quality, and reproducibility of statistical deliverables. The role requires oncology clinical trial experience, working knowledge of CDISC standards, and collaboration with internal study teams and relevant functional partners.

The contractor is expected to be available during core U.S. business hours, generally 9:00 a.m.–3:00 p.m. Eastern Time, to interact with U.S.-based study teams.

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. It has over 28 years of experience and more than 4,000 professionals in over 20 countries across the Americas, Europe, and Asia-Pacific. The company emphasizes employee development, continuous training, diversity, and inclusivity.

Requirements

• Demonstrated experience supporting Phase 2 and Phase 3 oncology clinical trials, including event-driven and response-based endpoints.
• Experience reviewing clinical trial data to identify inconsistencies, missing data, unexpected patterns, or issues requiring follow-up.
• Working knowledge of CDISC standards, including SDTM and ADaM.
• Strong written communication skills, including the ability to summarize findings, recommendations, and data issues for study team review.
• Strong analytical skills and a methodical approach to data review, statistical output review, and issue identification.
• Ability to collaborate with study teams, programming teams, and relevant functional partners.
• Solid understanding of statistical analysis methodology and principles of experimental design.
• Proficiency with statistical programming and data processing software, such as SAS and/or R.
• PhD or equivalent degree in statistics, biostatistics, or a related discipline with at least 3 years of relevant work experience; or a master’s degree with at least 6 years of relevant work experience.
• Availability during core U.S. business hours, generally 9:00 a.m.–3:00 p.m. Eastern Time.

Responsibilities

• Support statistical analyses of oncology endpoints, including time-to-event and response-based endpoints.
• Perform event projections to estimate the timing of planned event-driven analyses.
• Review and provide feedback on SDTM and ADaM specifications, tables, listings, figures, statistical analysis plans, protocol amendments, and relevant study documentation.
• Conduct routine study data review to identify inconsistencies, missing data, or other issues that may affect analysis or interpretation.
• Validate statistical outputs and provide documentation supporting reproducibility and quality control.
• Document review findings, assumptions, queries, and follow-up items clearly, and track issues through resolution.
• Collaborate with study teams, programming teams, and relevant functional partners to support timely resolution of data and analysis-related questions.

What This Job Offers

• Career Level: Senior
• Education Level: Ph.D. or professional degree