Lead programming and operational activities for clinical studies from study start to post-database lock, including database builds in Rave and Veeva, validation, system administration, vendor coordination, training, forecasting and SOP maintenance. Requires minimum 8 years' experience, strong OOP skills (C#, C++, VBS), CDISC knowledge and professional English; oncology experience preferred.

Lead programming and operational study teams to design, build, test, validate and support clinical databases and related applications (EDC: Rave, Veeva). Requires minimum 8 years' experience, strong knowledge of CDISC standards (CDASH/SDTM/ADaM), proficiency with multiple CDMS, experience in oncology preferred, object-oriented programming (C#, C++, VBScript), SOPs, validation documentation, project forecasting and stakeholder communication.

Full-time permanent remote position (Europe/Serbia) to manage programming aspects of clinical databases from study start through post-database lock. Role includes building/supporting clinical databases, developing and validating programs, system administration, producing validation documents, leading operational teams, project forecasting, and delivering trainings; experience with CDISC standards and object-oriented programming required.

The Principal Database Programmer manages programming aspects of clinical databases from study start through post-database lock for assigned projects. Responsibilities include building and supporting clinical databases, developing and validating programs, system administration, troubleshooting, preparing validation documents, participating in vendor selection and EDC demos/trainings, providing operational leadership and training, project forecasting and resource planning. Requires minimum 8 years' experience, strong Rave and Veeva experience, familiarity with CDISC standards (CDASH/SDTM/ADaM), proficiency in OOP languages (e.g., C#, C++ , VBS) and professional English. Oncology experience preferred.

Lead operational study and programming teams to develop, test, validate and maintain clinical databases and related applications per regulatory and SOP requirements. Requires minimum 8 years' experience, strong experience with Rave and Veeva, familiarity with CDISC standards (CDASH/SDTM/ADaM), object-oriented programming (C#/C++/VBS), and experience in oncology (autoimmune a plus). Role includes project forecasting, training, vendor/client communication and occasional travel.

Lead development and optimization of clinical data systems and ETL pipelines; drive enterprise data standardization (CDISC), build validation frameworks, ensure regulatory compliance (GCP, FDA 21 CFR Part 11), develop dashboards and analytics, mentor junior engineers, and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs across LATAM.