Associate Director of Statistical Programming

Job Summary

Providing statistical programming support for clinical trials, the full-time remote Associate Director of Statistical Programming will serve as the study lead programmer, ensuring high-quality deliverables from statistical vendors and collaborating closely with study teams on data analyses and cleaning activities.

Key responsibilities:

• Serve as the study lead programmer for assigned clinical trial(s), collaborating with study statisticians and data management
• Review and ensure high quality of Define packages and integrated datasets for regulatory submissions
• Perform independent validation of statistical vendor deliverables and support data cleaning activities with Clinical Data Management

Required qualifications:

• Master's Degree in Biostatistics, Statistics, Computer Science, or a related field with at least 12 years of experience in statistical programming for clinical trials
• Deep understanding of data standards and experience with Pinnacle 21 validation reports and Define XML packages
• Proficient in SAS and statistical computational software, including advanced data steps and analysis procedures
• Demonstrated ability to collaborate effectively with biostatisticians and cross-functional teams
• Strong organizational and project management skills, with the ability to manage multiple projects in a fast-paced environment