Lead Statistical Programmer - CDISC SDTM/ADaM Expert

Atlas Search; United States; On-site; USD 120,000 - 180,000; Full time

Job summary

Atlas Search is seeking a Senior Statistical Programmer to independently lead programming activities for assigned clinical studies while hands-on in programming, validation, and oversight of datasets, tables, listings, figures, and regulatory deliverables.

You will develop/validate SDTM and ADaM datasets using SAS and R, review vendor deliverables, ensure CDISC compliance, and collaborate with Biostatistics, Data Management, and Clinical Operations to meet study timelines and regulatory

Qualifications

• Lead study-level programming activities and timelines.
• Develop, program, and validate SDTM and ADaM datasets, tables, listings, and figures using SAS and, where appropriate, R.
• Collaborate with Biostatistics, Data Management, Clinical Operations, and cross-functional teams to clarify requirements and resolve issues.
• Review programs, datasets, outputs, and regulatory submissions for accuracy, traceability, and CDISC compliance.

Responsibilities

• Lead study-level programming activities, including planning and timeline management.
• Develop, validate SDTM/ADaM datasets and related outputs using SAS and R.
• Coordinate with cross-functional teams to resolve data and specification issues.
• Oversee vendor deliverables and support regulatory submissions.

Skills

Statistical programming

SDTM/ADaM

Vendor oversight

Cross-functional collaboration

Education

Bachelor’s degree in Statistics or related field

Tools

SAS

R

Job description

Atlas Search is seeking a Senior Statistical Programmer to independently lead programming activities for assigned clinical studies while hands-on in programming, validation, and oversight of datasets, tables, listings, figures, and regulatory deliverables.

You will develop/validate SDTM and ADaM datasets using SAS and R, review vendor deliverables, ensure CDISC compliance, and collaborate with Biostatistics, Data Management, and Clinical Operations to meet study timelines and regulatory