Statistical Programmer : Contribute to Clinical Research Excellence

Position: Statistical Programmer I: Contribute to Clinical Research Excellence
Launch your career in clinical research as a Statistical Programmer I. Engage in SAS programming and contribute to vital data management in a fully remote or on-site setting.

This position involves statistical programming as part of clinical trials, including the development of dataset specifications and performing conformance checks to ensure regulatory compliance. You will generate key statistical outputs, help clean data, and document your work meticulously according to industry standards. Perfect for individuals with strong analytical skills and a background in statistics.

Key Responsibilities:

• Review and develop dataset specifications for clinical trials

• Validate datasets and ensure CDISC compliance

• Create statistical output reports from trial data

• Assist in data cleaning and integrity checks

• Maintain documentation per quality assurance standards

Requirements:

• Master’s or Ph.D. in statistics or related disciplines

• SAS certification is required

• Familiarity with clinical trial programming preferred

• Strong analytical and problem-solving skills

• Commitment to maintaining quality standards

Make a significant impact in clinical research by applying your statistical expertise in this exciting role.
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