Clinical Database Programmer (Remote)

Due to growth we have a requirement for 10 Senior/Clinical Database Programmers to join our global team.

The candidate will be responsible for integrating data from IRT, EDC, and ECOA systems into a Data Visualization platform, building out data listings and creating analytics, such as reports and dashboards, based on that data. This role requires a strong technical understanding of these platforms and the ability to transform data into meaningful insights.

​This is a full-time permanent position based in any of the following CEE locations:

• Serbia
• Croatia
• North Macedonia
• Bosnia & herzegovina

Essential Functions/Responsibilities

• Program simple to complex data review listings, exception reports, QTL/KRIs, metrics reports and visualizations in a fast-paced environment for clinical trial data review and management purposes.
• Liaise with Clinical Data Management and/or cross functional staff to understand the needs of the end users of the listings, reports, and metrics.
• Contribute to the development of software systems and related infrastructure to generate displays of clinical study data and metrics reports that are efficient and user-friendly.
• Create and document archives of software and deliverables.
• Create any Work Instructions process, and training documents needed related to clinical programming and the required deliverables.
• Provide time and resource estimates for project planning as well as accurately record time spent on multiple deliverables.

Required Knowledge, Skills, and Abilities

System Experience:

• Focus on Data Listings and Custom Analytics: One of our key areas of need is building data listings directly from the EDC system.
• Custom analytics capabilities, including report building and report programming, to facilitate tailored data analysis for our projects.
• EDC (Electronic Data Capture): Proficiency in platforms such as Medidata RAVE and Veeva EDC is essential.
• IRT (Interactive Response Technology): Familiarity with systems like Yprime and endpoint is preferred.
• Experience with Clario ECOA is desirable.
• Skilled in programming in a relational database setting with SQL and/or T-SQL or ETL.
• Experience with data reporting tools in a clinical trial setting.
• Experience in the Biotechnology, Pharmaceutical, or Life Sciences industries (Clinical Research Organization – CRO or Clinical Trial regulated environment preferred).
• Experience with the eClinical Solutions.
• Familiarity with CDISC standards, including CDASH and SDTM.
• Experience with Data Visualization packages (Elluminate, Power BI, Spotfire, Qlik Sense and Tableau).
• Experience in the Biotechnology, Pharmaceutical, or Life Sciences industries (Clinical Research Organization – CRO or Clinical Trial regulated environment preferred).

Educational/Experience Requirements:

• Bachelor’s degree or equivalent in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields.
• Junior role- Minimum of 2-4 years of experience in a data visualization role.
• Senior role- Minimum of 5 years of experience in a data visualization role.