eCOA - Clinical Study Build Programmer

Role: Clinical Study Build Programmer - eCOA, responsible for designing, programming, testing, and implementing clinical data collection databases for global trials. Core responsibilities include configuring eCOA/EDC platforms, developing study forms, ensuring data standards, supporting data submission and regulatory activities, and collaborating with Data & Analytics teams to deliver accurate, efficient data systems aligned with study objectives. Requirements: Master's in Informatics, Life Sciences, or related; 3+ years in clinical data management or equivalent experience in data analytics, statistics, or IT; proficiency in clinical data systems, data standards, and programming. Preferred: Experience with eCOA data flow, clinical development knowledge, familiarity with data tools, and international travel readiness. High-value specifics: supportive of multiple therapeutic areas, clinical trial phases (preclinical to Phase 3), regulatory compliance (ICH, GCP, FDA), and technical platforms involved in global data collection efforts. Reporting to project leaders, with a focus on process improvement and risk management in a GxP environment. Work setup: not specified but implies collaboration across global teams and potential international travel.