Programmer Analyst/Sr Programmer Analyst (Centralized Monitoring/RBQM)
Core
Lead programmer for moderately complex clinical trials studies, performing advanced bioinformatics programming, data integration, and validation for statistical and computational research projects.
Role type
Senior IC clinical data programmer (bioinformatics)
Builds
Validated programs for data transfer, combination, summary generation, and reporting (listings, tables, figures) within clinical trial environments.
Domain
Clinical trials / Pharmaceutical industry / Bioinformatics
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming, data integration, relational database structure, biostatistical metrics capture, quality control review, training and mentoring
Preferred skills
Centralized Monitoring, Risk-Based Quality Management (RBQM), data visualization (Spotfire, Tableau, Power BI, R Shiny), Python, R, SQL, Snowflake
Technologies
SAS, Spotfire, Tableau, Power BI, R Shiny, Python, R, SQL, Snowflake
Responsibilities
Lead programming on moderate complexity studies; create, execute, maintain, and validate programs for data transfer and reporting; manage assignments to meet timelines; provide training and guidance to junior team members; support bidding processes.
Seniority
Senior, hands-on IC with mentorship responsibilities