Senior Biostatistician

United Consulting Hub; United States; Remote; USD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking two Senior Biostatistician Consultants for a dynamic 6-month remote engagement. This role is perfect for professionals with extensive experience in regulatory submissions and statistical programming. You'll collaborate closely with programming teams, providing statistical guidance and ensuring accuracy in data outputs. Strong communication skills are essential to translate complex data insights to cross-functional teams. If you're looking to make a significant impact in a fast-paced environment, this opportunity is for you!

Qualifications

• 8–10+ years of biostatistics experience in the pharmaceutical industry.
• Strong programming expertise with TLF generation.

Responsibilities

• Support regulatory submission efforts with statistical analysis.
• Draft Statistical Analysis Plans and review TLFs.

Skills

Biostatistics

Statistical Programming

CDISC Standards

Regulatory Submissions

Communication Skills

Education

MS in Biostatistics

MS in Statistics

Tools

Statistical Software

Job description

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Duration: 6 Months (Contract, with potential for extension)

Position Summary:

A leading pharmaceutical company is seeking two experienced Senior Biostatistician Consultants for a 6-month, potentially renewable engagement. This is a remote, hands-on role ideal for professionals with a solid background in regulatory submissions, statistical programming (including TLFs), and CDISC standards. Strong communication skills are essential for success in this collaborative, fast-paced environment.

Key Responsibilities:

• Support regulatory submission efforts with hands-on statistical analysis.
• Draft Statistical Analysis Plans (SAPs) and perform comprehensive reviews of Tables, Listings, and Figures (TLFs).
• Collaborate closely with programming teams, providing statistical guidance and ensuring accuracy of outputs.
• Interpret data findings and communicate insights effectively to cross-functional teams.

Required Qualifications:

• 8–10+ years of biostatistics experience within the pharmaceutical industry, including recent sponsor-side roles.
• Minimum of an MS degree in Biostatistics or Statistics.
• Strong programming expertise with TLF generation and familiarity with CDISC standards.
• Proven experience contributing to successful regulatory submissions.
• Excellent written and verbal communication skills with the ability to translate complex data for non-technical audiences.

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Other

Industries

• Pharmaceutical Manufacturing

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