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Clinical Database Programmer Jobs in Raleigh, NC

Senior Data Engineer

Raleigh, NC · On-site

$91K - $163K/yr

Use enterprise-approved AI tools to automate data engineering workflows, streamline ETL maintenance ... clinical or real-time analytics * Experience with ETL orchestration tools (e.g., Airflow, Azure ...

Senior Data Engineer

Raleigh, NC · Remote

$91K - $163K/yr

Use enterprise-approved AI toolsto automate data engineering workflows, streamline ETL maintenance ... clinical or real-time analytics * Experience with ETL orchestration tools (e.g., Airflow, Azure ...

Data Architect-ADF

Raleigh, NC · On-site

$62 - $79.75/hr

Knowledge of Azure DevOps, CI/CD is a plus * Experience in data modeling and database design with ... Good understanding of clinical trial business domain * Data modeling experience in the clinical ...

With the help of our extensive database of internal candidates and CATS applicants tracking system ... Clinical, etc. for both our commercial and government clients. Recruitment Process: * Source: A ...

Senior Salesforce Developer

Raleigh, NC · On-site

$122K - $149K/yr

... and clinical partners to deliver high-quality, scalable, and outcomes-focused products. The ... Use variables, databases, arrays, and/or data frames. * Configure and use APIs and web services.

New

Principal Software Engineer (Backend)

Raleigh, NC · On-site

$131K - $175K/yr

NET WebAPI, WCF, REST • 5+ yrs. in relational database development • 5+ yrs. in version control ... Veradigm is an integrated data systems and services company that combines data-driven clinical ...

Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the ... databases, websites, etc.). • Manages the review/approval of electronic test requests and ensures ...

Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the ... Agile, databases, websites, etc.). Manages the review/approval of electronic test requests and ...

... Engineering, professional, Scientific & Clinical, etc. for both our commercial and government ... Experience with Oracle database technology * Able to work independently to achieve outcomes in an ...

Software Development Engineer III

Durham, NC · On-site +1

$85K - $140K/yr

Strong database design and query writing using SQL Server or RDBMS systems. * Well versed in API ... Understanding of clinical laboratory operations or healthcare IT environments. * Experience with ...

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Showing results 1-20

Clinical Database Programmer information

See Raleigh, NC salary details

$67.6K

$115.6K

$206.1K

How much do clinical database programmer jobs pay per year?

As of Jun 30, 2026, the average yearly pay for clinical database programmer in Raleigh, NC is $115,634.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,800.00 and $175,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Clinical Database Programmer position, and why are they important?

To excel as a Clinical Database Programmer, you need a bachelor's degree in computer science or a related field, experience in database design, and a strong understanding of clinical data standards. Proficiency in database management systems (such as Oracle or SQL), knowledge of electronic data capture (EDC) tools like Medidata Rave, and familiarity with programming languages like SAS or SQL are commonly required, along with certifications such as CDISC or Medidata Solutions. Attention to detail, problem-solving ability, and strong communication skills are valuable soft skills for this role. Mastering these competencies is vital for ensuring high-quality, regulatory-compliant clinical trial data and effective collaboration within multidisciplinary research teams.

What is a Clinical Database Programmer job?

A Clinical Database Programmer is responsible for designing, developing, and maintaining databases used in clinical trials. They ensure that data is collected, stored, and managed efficiently while complying with regulatory standards such as CDISC and FDA guidelines. Their role involves creating database structures, writing validation checks, and supporting data analysis to ensure accurate and reliable clinical trial results. They often work with clinical data managers, biostatisticians, and regulatory teams.

What are common responsibilities and team interactions for a Clinical Database Programmer in a typical workweek?

As a Clinical Database Programmer, your primary responsibilities usually include designing, building, and validating clinical trial databases, ensuring data is collected and managed in compliance with industry standards and regulatory requirements. You will frequently collaborate with clinical data managers, biostatisticians, and study coordinators to define data collection requirements and resolve data discrepancies. Team meetings and cross-functional communication are integral parts of the role, as you work together to maintain database integrity throughout the study lifecycle. This collaborative environment provides valuable experience in both technical problem-solving and teamwork, often paving the way for advancement into senior programming or data management positions.

What are popular job titles related to Clinical Database Programmer jobs in Raleigh, NC? For Clinical Database Programmer jobs in Raleigh, NC, the most frequently searched job titles are:
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What cities near Raleigh, NC are hiring for Clinical Database Programmer jobs? Cities near Raleigh, NC with the most Clinical Database Programmer job openings:
Infographic showing various Clinical Database Programmer job openings in Raleigh, NC as of June 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $115,634 per year, or $55.6 per hour.
Epidemiological Programmer, Real World Evidence - FSP (Sponsor - Dedicated)

Epidemiological Programmer, Real World Evidence - FSP (Sponsor - Dedicated)

IQVIA

Durham, NC • On-site

$88K - $220K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

53rd of 207 rated it services


Job description

IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. Epidemiological Programmer role sits within our Real World Solutions team and will be responsible for leading development of datasets and conducting longitudinal analyses for observational studies in the virology therapeutic area under one client portfolio. It is important for this individual to have demonstrated experience and applied proficiency in observational research utilizing EMR and claims data, a strong statistical programming skillset, both knowledge and applied experience with epidemiological study design, terminology, cohort building, and RWE outcome measures, and experience managing multiple studies and complex analyses. In this role, individuals will have access to real-world databases and act as the stewards of the client's best practices, standards, and methodologies underlying the use of real-world data (RWD).

Essential Functions

  • Lead development of analytic datasets through raw data processing and conduct data checks / cleaning using secondary real world data sources, including claims, EHR, and lab data (e.g. Optum, HealthVerity, TriNetX, IQVIA PharMetrics Plus)

  • Lead the feasibility of real-world data sources to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives.

  • Conduct and QC analyses, including identification of diagnosis and treatment codes and applying statistical methods to handle censored data, confounding, differing person-time, and missing data

  • Collaborate with epidemiologists on study design and methodology, as well as define specifications for descriptive and complex statistics (e.g. longitudinal analysis, survival analysis, regression models, propensity score methods) in studies using RWD for virology research questions

  • Develop and QC TFLs for protocols/reports/manuscripts using RWD (e.g. claims and EHR)

  • Support development of other study documents including protocols, statistical analysis plans, and study reports

  • Communicate timelines, progress reports, and results to project team and key stakeholders

  • Provide technical, programming, statistical, and epidemiological expertise and independently bring project solutions to team for complex studies

Qualifications

  • Master's Degree in Biostatistics, Epidemiology, Outcomes Research or related field with 5-8 years relevant experience or PhD with 3 years relevant experience required

  • Strong track record of analysis of RWD using EMR and claims data

  • Demonstrated proficiency in advanced statistical programming using SAS and/or R, macros, SQL required

  • Demonstrated experience and applied proficiency of RWE study design, terminology, cohort building, and analytic methodologies

  • Prior pharmaceutical experience

  • Excellent analytic and communication skills with attention to detail

  • Ability to effectively manage and prioritize multiple tasks and projects

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 athttps://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.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US