Senior Principal Programmer, Atlanta, GA
HybridAtlanta, Georgia, United States
Job Summary
Review and coordinate clinical trial analysis and reporting setup requests to ensure accuracy and timely delivery. Configure study structures, repositories, datasets, and access controls in line with CDISC and governance requirements. Manage role-based access and Git/Azure DevOps resources while coordinating environment provisioning with platform administrators. Support programming teams during onboarding, system transitions, and daily operations as a first-line technical contact. Improve lifecycle management by documenting processes, supporting validation activities, and automating practical solutions. Work with statistical programming teams, Biometrics partners, and stakeholders to translate clinical needs into well-governed study setups. Hybrid schedule with 40% office time; 5+ years of clinical trial results generation experience required.
Required Qualifications
- 5+ years of experience in clinical trial results generation, reporting, and submission processes
- experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements
- understanding of CDISC standards, including SDTM and ADaM, and experience with Tables, Figures, and Listings
- experience in regulated pharmaceutical environments with understanding of SDLC, validation, audit readiness, and compliant configuration expectations
- ability to communicate clearly with technical teams and business stakeholders while tracking setup processes across systems and teams
- practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio
- hybrid work arrangement with 40% of time spent in the office
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