Clinical Programmer I / II
Core
Design and deliver data solutions, including SAS/Python/R/SQL programming and Power BI/Spotfire dashboard development, to process clinical trial data and generate actionable insights for study teams.
Role type
Individual Contributor Clinical Programmer
Builds
Production data programs, dashboards, and automated reporting tools for clinical trials
Domain
Life Sciences / Clinical Trials / Data Engineering
Required skills
SAS, Python, R, SQL, Power BI, Spotfire, Data Modeling, Data Cleaning, Report Development, Validation, EDC Systems
Preferred skills
FDA regulations, GCP/ICH guidelines, MicroStrategy, Clinical Development Process
Technologies
SAS, Python, R, SQL, Power BI, Spotfire, MicroStrategy, Medidata Rave, Inform, Veeva, Saama, Entimice, SAS LSAF
Responsibilities
Design, develop, and validate programs to process and report clinical trial data; Build, validate, and maintain dashboards for internal and external users; Automate manual checks and create tools to reduce data errors; Program operational reports to track data cleaning status and study readiness; Develop visualizations to highlight discrepancies between EDC and TPV data; Work within established frameworks and SOPs to ensure data quality and documentation.
Seniority
Mid-level Individual Contributor