Senior Statistical Programmer - Flexible Hours & SAS Expert

Automatic Data Processing, Inc.; Durham (NC); On-site; USD 90,000 - 125,000; Full time

Job summary

Total Trials, Inc. is seeking a Senior Statistical Programmer to lead SAS-based programming for clinical projects, ensuring alignment with ICH GCP, regulatory requirements, and trial protocols.

You will develop and maintain SAS programs, provide input on tables, listings, and graphs, deliver CDISC-aligned datasets, and support TMF documentation across cross-functional teams. Strong communication and problem-solving skills are essential; 4+ years in statistical programming in a clinical setting

Qualifications

• Graduate or post-graduate degree in science, biotechnology, or related field, or equivalent combination of education and experience.
• Minimum of four (4) years' experience in statistical/database programming within a clinical research setting.
• Proficiency in SAS; working knowledge of R is advantageous

Responsibilities

• Perform database programming, including derived items, automated edit checks, and customized reports.
• Conduct pre-processing and post-processing of imported and exported data
• Perform data quality checks and validation
• Provide input into and/or assist with: Statistical tables, listings, and graph templates; Statistical reports; Data review activities through programming support
• Produce and deliver: Derived datasets, tables, listings, and figures; Post-processed datasets aligned with CDISC standards
• Develop, maintain, and validate SAS macros
• Provide biometrics programming support to internal stakeholders and clients
• Support preparation and review of procedural documents and Trial Master File documentation
• Any other duties and responsibilities as may be assigned from time to time

Skills

English communication

Attention to detail

Organizational skills

Problem solving

Software tools proficiency

Interpersonal skills

Regulatory knowledge

Education

Graduate or post-graduate degree in science/biotech or related field

Tools

SAS

R

Job description

Total Trials, Inc. is seeking a Senior Statistical Programmer to lead SAS-based programming for clinical projects, ensuring alignment with ICH GCP, regulatory requirements, and trial protocols.

You will develop and maintain SAS programs, provide input on tables, listings, and graphs, deliver CDISC-aligned datasets, and support TMF documentation across cross-functional teams. Strong communication and problem-solving skills are essential; 4+ years in statistical programming in a clinical setting