Senior Clinical Data Analytics & Reporting Programmer

5PY IQVIA RDS Inc.

Durham (NC)

On-site

USD 88,000 - 221,000

Full time

5 days ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

IQVIA is seeking an experienced Clinical Data Analytics & Reporting Programmer to lead development of analytics, reporting, and data visualization solutions for global clinical trials.

You will partner with cross-functional stakeholders to transform complex clinical data into actionable insights that drive monitoring, risk-based approaches, data review, and decision-making initiatives.

Qualifications

  • Bachelor's degree in a relevant field.
  • 4+ years in analytics-focused roles with data warehouse experience in regulated environments.
  • Advanced data visualization and dashboard development using Spotfire or similar BI platforms.
  • Strong programming experience with Python, R, SAS, or similar languages.
  • Experience gathering business requirements and translating them into requirements docs.
  • Strong understanding of clinical trial data structures, including SDTM.

Responsibilities

  • Lead the design, development, and delivery of clinical reporting, dashboards, visualizations, metrics, and analytical solutions.
  • Partner with stakeholders to gather requirements and translate them into scalable reporting/analytics solutions.
  • Mentor team members and provide technical leadership on reporting and analytics practices.
  • Drive process improvements and innovative approaches to clinical data reporting/analytics.
  • Serve as SME for clinical data analytics, visualization platforms, and reporting technologies.
  • Independently manage complex assignments and deliver high-quality solutions.

Skills

Data visualization
Programming
Requirements gathering
SDTM knowledge

Education

Bachelor's degree in Computer Science, Engineering, Statistics, Life Sciences, or related discipline

Tools

Spotfire

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.

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.

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Clinical Data Analytics & Reporting Programmer
Senior Clinical Data Analytics & Reporting Programmer

IQVIA • Durham (NC)

On-site
USD 88,000 - 221,000
Clinical Trial Feasibility Analyst
Clinical Trial Feasibility Analyst

IQVIA • Durham (NC)

Remote
USD 88,000 - 221,000
Trial Clinical Delivery Lead- Oncology
Trial Clinical Delivery Lead- Oncology

QPL IQVIA RDS Poland Sp. z o.o. • Durham (NC)

On-site
USD 103,000 - 286,000
Senior Standards Engineer
Senior Standards Engineer

IQVIA • Durham (NC)

On-site
USD 98,000 - 273,000
Biostatistics Director- Global BIOS
Biostatistics Director- Global BIOS

5PY IQVIA RDS Inc. • Durham (NC)

Hybrid
USD 135,000 - 376,000
Competitive Intelligence Consultant, Strategy/Life Sciences
Competitive Intelligence Consultant, Strategy/Life Sciences

IQVIA • Wayne (PA)

On-site
USD 89,000 - 223,000
Clinical Trial Feasibility Analyst
Clinical Trial Feasibility Analyst

Regulatory Toolkit • United States

Remote
USD 88,000 - 221,000
Staff Software Development Engineer · IT Design & Development
Staff Software Development Engineer · IT Design & Development

IQVIA INC (US10) • Wayne (PA)

On-site
USD 103,000 - 288,000
Clinical FSP Quality Manager
Clinical FSP Quality Manager

5PY IQVIA RDS Inc. • Durham (NC)

On-site
USD 63,000 - 216,000
Sr. Clinical lead
Sr. Clinical lead

IQVIA • Durham (NC)

On-site
USD 93,000 - 233,000