Senior Clinical Data Analytics & Reporting Programmer
About The Position
IQVIA is seeking an experienced Clinical Data Analytics & Reporting Programmer to lead development of advanced analytics, reporting, and data visualization solutions supporting global clinical trials. The role partners with cross-functional stakeholders to turn complex clinical data into actionable insights that support medical monitoring, risk-based monitoring, data review, and clinical decision-making. The position provides technical leadership and subject matter expertise in clinical data analytics, visualization platforms, and reporting technologies. The successful candidate independently manages complex assignments, mentors team members, and advances reporting and analytics practices in a regulated clinical-trial environment. IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. It aims to accelerate the development and commercialization of medical treatments and improve patient outcomes and population health. IQVIA is an equal opportunity employer and maintains a zero-tolerance policy for candidate fraud. The annualized potential base pay range is $88,300.00–$220,900.00. Actual base pay may vary based on qualifications, location, and schedule. Depending on the position offered, incentive plans, bonuses, and other compensation may be offered, along with health, welfare, and other benefits.
Requirements
- Bachelor's degree in Computer Science, Engineering, Statistics, Life Sciences, or a related discipline.
- At least 4 years of experience as a Business Analyst, Clinical Data Analyst, or in a similar analytics-focused role working with data warehouse environments in a regulated industry and clinical trial setting.
- Advanced expertise in data visualization and dashboard development using TIBCO Spotfire or comparable business intelligence platforms.
- Strong programming experience with Python, R, SAS, or similar analytical scripting languages.
- Experience gathering business requirements and developing user requirements documentation.
- Strong understanding of clinical trial data structures, including SDTM.
Nice To Haves
- At least 6 years of relevant experience in clinical data analytics, reporting, or business intelligence within pharmaceutical, biotechnology, or life sciences organizations.
- Knowledge of CDISC standards and clinical data standards implementation.
- Experience mentoring, coaching, and developing junior team members.
- Demonstrated ability to apply advanced technical and problem-solving skills to deliver innovative solutions that improve operational efficiency.
- Experience serving as a technical subject matter expert in clinical data analytics, reporting, or therapeutic area-specific domains.
Responsibilities
- Lead the design, development, and delivery of clinical reporting, dashboards, visualizations, metrics, and analytical solutions.
- Partner with business stakeholders to gather requirements and translate them into scalable reporting and analytics solutions.
- Mentor team members and provide technical leadership on reporting, visualization, and analytics best practices.
- Drive process improvements and innovative approaches to clinical data reporting and analytics.
- Serve as a subject matter expert for clinical data analytics, visualization platforms, and reporting technologies.
- Independently manage complex assignments and deliver high-quality solutions with minimal oversight.
Benefits
- Health and welfare benefits may be offered, depending on the position.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
