Statistical Programmer Contractor

Statistical Programmer Contractor ProKidney Winston-Salem, NC Job Details Contract 22 hours ago Qualifications Project reporting Biotechnology Statistics Document review (document control) Statistics Computer Science Biostatistics SAS Mathematics Project timeline management SAS language Master's degree Analysis skills Bachelor's degree Quality control CDISC standards Master's degree in statistics Master's degree in mathematics Regulatory submissions Master's degree in computer science Data validation Clinical research documentation Senior level Cross-functional collaboration Communication skills Project stakeholder communication Cross-functional communication Statistical analysis tools 10 years

Full Job Description Statistical Programmer Contractor Position Summary:

The Statistical Programmer Contractor is responsible for developing, validating, and maintaining SAS programming deliverables to support clinical study analysis and reporting. This role collaborates closely with Biostatistics and other cross-functional team members to produce high-quality, compliant datasets, tables, listings, and figures while ensuring adherence to project timelines, SOPs, regulatory requirements, and CDISC standards.

Responsibilities:

Program and validate tables, listings, figures, and derived datasets using SAS. Develop SDTM and ADaM datasets and supporting documentation. Prepare and review mapping specifications and annotated case report forms (CRFs). Perform quality control and validation activities for programming deliverables. Collaborate with study team members to identify, investigate, and resolve data and output issues. Review study documents and provide input to improve programming quality, efficiency, and consistency. Maintain complete, accurate, and audit-/inspection-ready programming documentation. Communicate project status, risks, issues, and timeline impacts clearly to stakeholders.

Qualifications:

Bachelor's degree required; Master's degree preferred in Statistics, Biostatistics, Mathematics, Computer Science, or a related field. Minimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry. Phase 3 and regulatory submission experience preferred. Strong SAS programming skills, with experience developing SDTM, ADaM, tables, listings, and figures. Strong knowledge of clinical trial processes, regulatory requirements, and programming documentation. High attention to detail, with strong analytical, problem-solving, and communication skills. ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.