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Job Title: Statistical Programmer 

Location: Remote

Contract Type: Contract

About the Role:

We are currently seeking a highly skilled Statistical Programmer with well-documented MMRM (Mixed-Effects Model for Repeated Measures) experience in clinical trials. This is an exciting opportunity for an experienced professional to contribute to impactful clinical research while working remotely.

The ideal candidate is proficient in statistical programming, has hands-on experience with MMRM in clinical trials, and can start immediately. If you are detail-oriented, excel in a fast-paced environment, and are eager to make a difference in clinical research, we encourage you to apply!

Key Responsibilities:

• Develop, validate, and maintain statistical programming code to support clinical trial data analysis.
• Implement MMRM models and other statistical methodologies in compliance with clinical trial protocols.
• Collaborate with statisticians, data managers, and clinical trial teams to ensure accurate and efficient programming solutions.
• Prepare and review programming deliverables, including analysis datasets, tables, listings, and figures (ADaM, SDTM, etc.).
• Ensure all programming deliverables meet regulatory and quality standards (e.g., FDA, ICH guidelines).
• Troubleshoot and resolve data issues and programming errors promptly.
• Document programming processes and maintain clear, reproducible code for audits and reviews.
• Contribute to database setup and ensure alignment with study objectives and analysis requirements.

Qualifications:

• 3+ years of statistical programming experience in the clinical trials or pharmaceutical industry.
• Strong proficiency in SAS programming and familiarity with other programming languages (e.g., R or Python) is a plus.
• Well-documented experience implementing and interpreting MMRM models in clinical trial data analysis.
• Solid understanding of clinical trial data structures, CDISC standards (SDTM/ADaM), and regulatory requirements.
• Strong knowledge of statistical methodologies used in clinical trials, including MMRM and other longitudinal data analysis techniques.
• Familiarity with regulatory submission requirements (FDA, EMA, etc.) and related documentation.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work independently in a remote environment while collaborating effectively with cross-functional teams.

Preferred Qualifications:

• Advanced degree (Master's or Ph.D.) in Statistics, Biostatistics, Computer Science, or a related field.
• Experience in programming for regulatory submissions and audits.
• Knowledge of additional statistical modeling techniques is a plus.