Biostatistics Consultant – Oncology Program

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🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

⏱ Part Time

🟡 Mid-level

🟠 Senior

💼 Consultant

👻 Ghost score 15%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Global Channel Management, Inc.

WebsiteLinkedInAll Job Openings

11 - 50 employees

💼 Consulting

🎯 Recruiter

☁️ SaaS

Consulting • Recruitment • SaaS

Global Channel Management, Inc. is a technology company that specializes in recruiting and staff augmentation services. With over a decade of experience, their account managers and recruiters help organizations address challenges in acquiring skilled talent, manage fluctuating skill needs, and reduce training and labor costs. They focus on providing companies with the best talent to meet various staffing needs and timelines across different verticals.

📋 Description

• Serve as the primary biostatistician for assigned oncology clinical studies • Manage study closeout activities • Review, validate, and execute complex statistical analyses • Partner with and guide statistical programmers on developing SDTM/ADaM datasets • Craft comprehensive TLF (Tables, Listings, and Figures) specifications • Perform stringent quality control checks on programming efforts • Interpret complex statistical results • Contribute statistical methodologies, text, and data structures for scientific abstracts, posters, and manuscripts • Collaborate with the Medical Strategy Lead and Publications Specialist on publication-related statistical questions • Clarify statistical ambiguity and present complex concepts to technical and non-technical stakeholders • Ensure accuracy and data integrity across data-driven insights • Align analysis metrics with clinical trial protocols and compliance requirements

🎯 Requirements

• Minimum of 3 years of post-PhD experience or 5 years of post-MS experience directly managing and executing statistical analyses within clinical trials • Deep knowledge of statistical principles, up-to-date methodologies, and complex design rules applied within oncology clinical trials • Hands-on experience with Bayesian modeling and analysis and traditional frequentist statistical frameworks • Expert-level proficiency in SAS and R • Ability to independently guide, validate, and troubleshoot automated analyses • Comprehensive experience with CDISC SDTM and ADaM data standards, including development and quality control of data specifications • Elite written and verbal communication skills • Ability to explain complex statistical designs, decision rules, and analysis plans to cross-functional medical teams • PhD or Master's degree (MS) in Statistics or Biostatistics

🏖️ Benefits

• Part-time consulting engagement • Flexible engagement capacity that scales from approximately 10–15 hours per week during Months 1–3 to 5–10 hours per week for the remaining term