New · posted Nov 5
IQVIA · Pharmaceuticals
Senior Clinical Data Analytics & Reporting Programmer
- Durham, NC
- On-site
- Full-time
- Senior & Principal
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.
What you need
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 Qualificationsnice to have
- 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 Candidatenice to have
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 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.
Skills named in this posting
What you'll do
- 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.
Pay and benefits
$88,300 – $220,900 a year
Employer providedHealth and welfare benefits
Incentive plans
Bonuses
Where you'll work
Durham, NCOn-siteOpen in Maps (opens in a new tab)
More jobs in Durham, NCEqual opportunity, accessibility and legal noticesIQVIA's statements, word for word
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
Job intelligence
The context around this role
Live data · November 5, 2026
Salary intelligence
How the pay compares
This role's midpoint is 8% above the US median for Clinical Data Management roles at this level.
This roleEmployer provided
Senior & Principal roles in the US17 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $88,300 | — | $220,900 |
| All US (middle half) | $126,500 | $142,500 | $154,500 |
This role: IQVIA's own published range. Comparisons: the base pay employers published on open Clinical Data Management roles at the same level on Regulatory Jobs, November 5, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Data Management
The general path across 62 open Clinical Data Management roles on Regulatory Jobs, with the titles they carry most. Not IQVIA's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 22 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct6
- Collaboration and leadership6
- Documentation and SOPs3
- Lab testing and methods2
- Validation and qualification1
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Data Management work in pharmaceuticals, led by the one this posting names, each linked to the agency or standards body that publishes it.
- CDISCCDISC standards(official source, opens in a new tab)SDTM, ADaM and CDASH, the clinical data standards FDA and PMDA requireNamed in the posting
- FDAFDA study data standards(official source, opens in a new tab)Required data standards and technical conformance for clinical study data
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- ICHICH E3(official source, opens in a new tab)Structure and content of clinical study reports
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- FDAFDA Electronic Submissions Gateway(official source, opens in a new tab)The agency-wide gateway for receiving electronic regulatory submissions
Company hiring pulse
IQVIA on Regulatory Jobs
- 87
- Open roles
- 61
- Distinct roles
- 28
- Locations
By discipline
- Clinical76 87%
- Regulatory7 8%
- Quality4 5%
By level
- Associate & Specialist45 52%
- Manager16 18%
- Senior & Principal16 18%
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Senior Clinical Data Analytics & Reporting Programmer at IQVIA
Open until filled. $88K–$221K a year, employer provided.