Clinical Database Programmer

Location : home-based in the U.S. or Canada

Summary :

IQVIA has formed a sponsor-dedicated team offering long-term dedication to a Rare Disease Biopharma company. We are seeking to hire a Clinical Database Programmer, at the senior level, to work fully on sponsor-side activities.

This individual will support the Data Management and Biostatistics departments for the sponsor, handling the EDC data build process.

Create test data in Rave EDC system.

Responsibilities :

Collaborates with peers, data management and statistics to ensure the quality and accuracy of EDC build process.

The development of programming scripts for data retrieval, transformation and representation as well as their validation.

Handles implementation and maintenance of internal data quality control programs, acceptance criteria for data from external sources and performs the related programming.

Leads the set-up and maintenance of a suite of reports that function as a sample report library for study teams to choose from in order to help them efficiently lead their projects.

Leads the implementation and organization of automated regular reports on study platforms and oversees correct processing of automated reports.

Collaborates with the clinical study team in developing ongoing data quality standards and clinical data acceptance rules for clinical data in the eCRF and related external data sources collecting data from clinical studies.

Qualifications :

Degree (BSc / MSc) in Computer Science, Mathematics / Statistics, or related area with relevant experience. Other degrees and certifications considered if commensurate with related data management and clinical programming experience.

5+ years of experience in the areas of clinical data management and / or clinical programming (working within a CRO or Pharmaceutical setting).

Working experience with Rave EDC is required.

Strong knowledge in CDISC standards (CDASH, SDTM) is required.

Understanding of data management and / or clinical programming processes and standards.

Knowledge in statistical programming using the SAS software or reports programming in reporting tools such as Business Objects or J-Review.

Ability to work effectively in a team setting, and to meet set goals by managing own timelines.

Ability to work in cross-functional, multicultural and international clinical trial teams.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.

We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn more at

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.

The potential base pay range for this role, when annualized, is $106,200.00 - $177,000.00. 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.