Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Core
Transform complex clinical trial data into actionable insights to advance Risk-Based Quality Management (RbQM) and Central Monitoring platforms.
Role type
Associate Clinical Programmer (Clinical Study Data, RbQM & Monitoring)
Builds
Central Monitoring Platform outputs, analytics dashboards, reports (KRIs, QTLs, DQA), and data pipelines.
Domain
Clinical trials, Risk-Based Quality Management, Data Analytics
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming, R/Python/SQL, data extraction/cleaning/merging, BI tools (Power BI/Spotfire/Tableau), clinical trial data structures, RbQM principles, KRI/QTL development
Preferred skills
CluePoints platform experience, CDISC standards (SDTM/ADaM), AI/ML knowledge
Technologies
SAS, R, Python, SQL, Power BI, Spotfire, Tableau, CluePoints
Responsibilities
Develop analytics dashboards and monitoring outputs; perform data extraction, cleaning, merging, and derivation; partner with study teams and statisticians; execute quality checks and validation routines; support dashboard refreshes and performance monitoring.
Seniority
Junior to Mid-level, hands-on IC