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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.
- Prepare dashboards, analytics summaries, risk reports, and data visualizations to clearly communicate findings to study teams and cross‑functional stakeholders.
Preferred skills & experience
- Hands‑on experience with CluePoints CM, KRI/QTL development, and Risk‑Based Quality Management (RBQM) frameworks.
- Strong understanding of clinical trial data structures, including SDTM, EDC‑derived datasets, operational metrics, and vendor‑sourced 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 https://jobs.iqvia.com
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. https://jobs.iqvia.com/eoe
IQVIA 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.
The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Learn more about this Employer on their Career Site
