Senior Clinical Data Analytics & Reporting Programmer

IQVIA
Location
Durham, North Carolina, United States of America
Job Type
Full-time
Posted
November 4, 2026
Salary Range
$88k - $221k USD

Job Description

About the Role

We are seeking an experienced Clinical Data Analytics & Reporting Programmer to lead the development of advanced analytics, reporting, and data visualization solutions supporting global clinical trials. This role partners with cross-functional stakeholders to transform complex clinical data into actionable insights that drive medical monitoring, risk-based monitoring, data review, and clinical decision-making initiatives.

Key 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.

Required Qualifications

  • Bachelor's degree in Computer Science, Engineering, Statistics, Life Sciences, or a related discipline.
  • 4+ years of experience as a Business Analyst, Clinical Data Analyst, or 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.

Preferred Qualifications

  • 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.

Ideal Candidate

The ideal candidate combines deep technical expertise in clinical data analytics with strong stakeholder engagement skills. You thrive in highly regulated environments, can independently solve complex business challenges, and have a proven track record of delivering impactful reporting and visualization solutions that support clinical development and decision-making.

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.

About the Role

We are seeking an experienced Clinical Data Analytics & Reporting Programmer to lead the development of advanced analytics, reporting, and data visualization solutions supporting global clinical trials. This role partners with cross-functional stakeholders to transform complex clinical data into actionable insights that drive medical monitoring, risk-based monitoring, data review, and clinical decision-making initiatives.

Key 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.

Required Qualifications

  • Bachelor's degree in Computer Science, Engineering, Statistics, Life Sciences, or a related discipline.
  • 4+ years of experience as a Business Analyst, Clinical Data Analyst, or 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.

Preferred Qualifications

  • 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.

Ideal Candidate

The ideal candidate combines deep technical expertise in clinical data analytics with strong stakeholder engagement skills. You thrive in highly regulated environments, can independently solve complex business challenges, and have a proven track record of delivering impactful reporting and visualization solutions that support clinical development and decision-making.

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.

Frequently Asked Questions

Where is this job located, and is there a remote option?
The job is located in Durham, North Carolina, United States of America. The posting does not specify a remote, hybrid, or on-site work policy.
What qualifications and experience are required for this position?
You need a Bachelor's degree in Computer Science, Engineering, Statistics, Life Sciences, or a related discipline, plus 4+ years of analytics-focused experience in a clinical trial setting and data warehouse environment. Required skills include advanced TIBCO Spotfire (or comparable BI) expertise, strong Python, R, or SAS programming skills, and a strong understanding of SDTM structures.
What are the key responsibilities of this role?
You will lead the design and delivery of clinical reporting, dashboards, and analytics solutions for global clinical trials. Duties include gathering requirements from business stakeholders, serving as a subject matter expert, mentoring team members, driving process improvements, and independently managing complex data assignments with minimal oversight.
What is the compensation range for this position?
The potential annualized base pay range for this role is $88,300.00 to $220,900.00. Actual base pay varies based on qualifications, experience, location, and schedule. Additional compensation may include incentive plans, bonuses, or other forms of pay depending on the position offered.
What benefits does IQVIA offer for this role?
IQVIA offers a range of health and welfare benefits, alongside potential incentive plans and bonuses, depending on the position offered.

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Job Information

Source: manual
AI Relevance: 85/100 (Highly relevant)
Remote Type: onsite
Skills & Tags:
iqvia clinical
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