Senior Clinical Database Programmer (Remote)

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

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

• Serbia
• Croatia
• North Macedonia
• Bosnia & herzegovina

As a Senior/Clinical Database Programmer you will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.

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 elluminate platform a plus
• Experience with Qlik Sense a plus.
• Preferred additional external data transfer experience in:
• Creating external data transfer specifications, ensuring external clinical trial data are compatible with the clinical database to support data integration, analysis and reporting.
• Experience in planning, set-up, and acquisition of external clinical data at the study level
• Liaising with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.)
• Knowledge of some additional programming languages (e.g.: SAS, PL/SQL, R, Python, Java)
• Ability to balance and prioritize multiple assignments and respond quickly to ad hoc requests.
• Familiarity with CDISC standards, including CDASH and SDTM.

Required/Preferred Education

• Bachelor’s degree or equivalent in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields.