Senior Clinical Programmer

This Clinical Programmer role at IQVIA supports RiskBased 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 CriticaltoQuality (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.
• Prepare dashboards analytics summaries risk reports and data visualizations to clearly communicate findings to study teams and crossfunctional stakeholders.

Preferred skills & experience

• Handson experience with CluePoints CM KRI/QTL development and RiskBased Quality Management (RBQM) frameworks.
• Strong understanding of clinical trial data structures including SDTM EDCderived datasets operational metrics and vendorsourced data.
• Proficiency in data analysis and programming tools including SAS (mandatory) SQL Python R Spotfire or equivalent analytical platforms.
• Ability to interpret complex analytical and statistical outputs and convert them into actionable insights

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.