Senior Clinical Programmer

Job description

This Clinical Programmer role at IQVIA supports Risk‑Based Quality Management by developing and validating KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring platform. The position blends programming and analytics to transform complex clinical and operational data into actionable insights, partnering closely with Clinical Monitoring, Data Management, Biostatistics, and RBQM leads. Strong clinical data expertise and proficiency in SAS and other analytical tools are essential for success. Key Responsibilities: - Develop and document requirements for the design of Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs) based on Critical‑to‑Quality (CtQ) factors and key study documents (e.g., protocol, CRF Completion Guidelines, data flow specifications). - Program, configure, and validate KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring (CM ) platform, ensuring accurate and reliable representation of study risks. - Collaborate closely with Clinical Monitoring, Data Management, RBQM Leads, Biostatistics, and Study Teams to translate analytical insights into actionable risk mitigation strategies and study interventions. - Prepar...