Endpoint Clinical is hiring a
Statistical Programmer

Summary

The Statistical Programmer is responsible for statistical activities in support of clinical trials and IRT implementation at Endpoint Clinical. The role requires a bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Sciences, or related subject area with 4+ years of statistical programming experience, preferably in processing clinical trial data. Experience in SAS, R, Python, and IRT platforms is required. Endpoint Clinical offers remote work.

Requirements

• Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Sciences, or related subject area is required
• 4+ years of statistical programming experience, preferably in processing clinical trial data
• Experience in statistical programming languages and software such as SAS, R, and Python required

Responsibilities

• Consult with clients on statistical approaches as required
• Write, modify, and maintain statistical programs and macros that produce randomization files, data sets, tables, and listings for assigned projects
• Review study protocols and randomization requirements to create and verify randomization and kit lists
• Ensure the integrity of the randomization process within the IRT system(s)
• Document and manage new and existing randomization lists
• Develop simulation programs to evaluate dynamic randomization models
• Review Statistical Analysis Plans and provide feedback to the author(s)
• Perform other duties as required and assigned

Preferred Qualifications

• SAS Certification(s) are highly preferred
• Prior experience in IRT platforms, eClinical technologies, life sciences, or regulated industries is highly preferred
• Knowledge of regulatory guidelines such as 21 CFR Part 11 and GxP

Benefits

Endpoint Clinical offers remote work