Senior Principal Programmer, Atlanta, GA

UCB•Atlanta, GA

24d•$148,000 - $194,000•Hybrid

About The Position

We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in Raleigh, NC or Atlanta, GA. You will help clinical programming teams move to and work confidently within UCB’s modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs. You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.

Requirements

Bachelor’s degree
Minimum of 5 years of experience in clinical trial results generation, reporting, and submission processes.

Nice To Haves

Experience with Domino Data Lab or other modern Statistical Computing Environments used in pharmaceutical research.
Experience supporting or administering Statistical Computing Environments (SCEs) within a pharmaceutical or regulated environment.
Knowledge of CDISC standards (SDTM, ADaM), statistical programming workflows, and clinical reporting outputs (TFLs).
Familiarity with platforms and tools such as Domino Data Lab, SAS, R, Python, Git, Azure DevOps, and SAS Studio.
Experience with computerized systems validation (CSV), SDLC, audit readiness, and compliant system deployment.
Demonstrated ability to author SOPs, training materials, and technical documentation, and deliver user training.
Strong project management, communication, and stakeholder engagement skills, with experience leading process improvement initiatives.
Evidence of technical leadership through industry presentations, publications, working groups, or professional organizations.

Responsibilities

Review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.
Configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.
Manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.
Coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.
Support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.
Improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.