Senior/Principal Statistician Consultant – TA, Oncology

🔥 3 minutes ago

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟠 Senior

💼 Consultant

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

📋 Description

• Provide statistical expertise and operational support for oncology clinical trial projects • 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 affecting analysis or interpretation • Validate statistical outputs and document reproducibility and quality control • Collaborate with internal study teams, programming teams, and relevant functional partners

🎯 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 • Ability to document review findings, assumptions, queries, and follow-up items clearly and track issues through resolution • Working knowledge of CDISC standards, including SDTM and ADaM • Strong written communication skills • 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 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

🏖️ Benefits

• Professional growth opportunities • Continuous training and development • Equal opportunity and diversity-focused workplace