Statistical Programmer

GQR; United States; Remote; USD 170,000 - 180,000; Full time

Job summary

A leading biopharmaceutical company seeks a Statistical Programmer Consultant to deliver clinical programming expertise for various therapeutic areas. This fully remote, full-time contract role offers the opportunity to contribute to studies from early to late phase clinical development. Candidates must have strong SAS skills and experience with CDISC standards, as well as excellent communication and organizational abilities.

Benefits

Medical insurance

Vision insurance

401(k)

Disability insurance

Paid maternity leave

Paid paternity leave

Qualifications

• Master's degree in Statistics, Computer Science, or related field.
• 1–5 years of relevant clinical programming experience.
• Strong SAS skills and understanding of CDISC standards.

Responsibilities

• Support statistical programming activities for clinical trials.
• Develop and QC SDTM/ADaM datasets and TLFs.
• Collaborate with cross-functional teams for quality deliverables.

Skills

SAS

CDISC standards

Statistical programming

Communication skills

Organizational skills

Education

Master's degree in Statistics

Master's degree in Computer Science

Job description

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

LinkedIn Top Voice | VP @ GQR | MIT AI/ML Certified Executive Recruiter | Built Teams for 100+ Biotech & Pharma Leaders | Getting You the Recognition…

Job Title: Statistical Programmer Consultant

Location: Remote – USA Only

NO C2C

Summary:

Our client, a leading biopharmaceutical company, is seeking a Statistical Programmer Consultant to provide clinical programming expertise across multiple therapeutic areas. This full-time contract position is fully remote and offers the opportunity to work on studies from early to late phase clinical development. The ideal candidate brings strong SAS skills and experience with CDISC standards in a regulated environment.

Responsibilities:

• Support statistical programming activities for clinical trials (Phases 1–3)
• Develop and QC SDTM/ADaM datasets and TLFs
• Collaborate with cross-functional teams to ensure quality and timely deliverables
• Contribute to process improvements and the development of statistical tools
• Create and review annotated CRFs for dataset mapping
• Serve as a point of contact for programming matters with internal and external teams

Qualifications:

• Master's degree in Statistics, Computer Science, or a related field
• 1–5 years of relevant clinical programming experience
• Proficient in SAS; experience with R or S-Plus is a plus
• Deep understanding of CDISC standards (SDTM, ADaM)
• Strong organizational and communication skills

Compensation:

$75/hour, 40 hours/week

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Contract

Job function

• Job function

  Research

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Paid maternity leave

Paid paternity leave

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