Senior Biostatistician

i-Pharm Consulting; United States; Remote; USD 130,000 - 150,000; Part time

Job summary

A leading consulting firm is seeking an experienced Biostatistician with a strong background in oncology and expertise in statistical analysis. This flexible remote role involves shaping clinical development strategies and provides a competitive salary. Ideal candidates will have over 10 years of experience and proficiency in SAS and R.

Qualifications

• 10+ years (MS) or 7+ years (PhD) in clinical drug development.
• Proven track record with NDA/BLA submissions is a plus.
• In-depth knowledge of FDA/ICH guidelines and CDISC standards.

Responsibilities

• Provide expert statistical input into clinical development plans.
• Interpret complex data into actionable clinical and regulatory insights.
• Support publications and scientific presentations as internal statistical lead.

Skills

Statistical Analysis

Oncology

Communication

Critical Thinking

Education

MS or PhD in Statistics, Biostatistics, Mathematics or related field

Tools

SAS

R

Job description

This range is provided by i-Pharm Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$100.00/hr - $140.00/hr

Direct message the job poster from i-Pharm Consulting

Are you a seasoned biostatistician with a passion for oncology and innovation?

Do you enjoy turning complex data into strategic clinical insights?

Looking for a flexible, remote role where your expertise truly shapes drug development?

If so, this opportunity may be exactly what you're looking for.

We’re seeking an experienced Biostatistician to play a pivotal role in shaping clinical development strategies. This is a remote, flexible position (30–40 hours/week) with core collaboration hours between 9 AM–3 PM EST.

What You'll Do

• Provide expert statistical input into clinical development plans, protocols, analysis plans, and regulatory submissions
• Interpret complex data and translate it into actionable clinical and regulatory insights
• Partner cross-functionally with clinical research, regulatory, data management, programming, and medical writing teams
• Support publications and scientific presentations as the internal statistical lead
• Champion innovative statistical methods to streamline development and enhance decision-making

What You Bring

• 10+ years (MS) or 7+ years (PhD) of experience in clinical drug development
• Strong background in oncology (solid tumours or hematologic malignancies)
• Proven track record with NDA/BLA submissions is a plus
• Proficiency in SAS, R, and other statistical programming tools
• In-depth knowledge of FDA/ICH guidelines, CDISC standards, and global regulatory expectations
• Strong communication skills, critical thinking, and collaborative spirit
• Desire to thrive in a fast-paced, forward-thinking environment

Education

MS or PhD in Statistics, Biostatistics, Mathematics, or a related field

Ready to apply your expertise where it truly matters?

We’d love to hear from you. Reach out to learn more or apply today.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science and Research

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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