A company is looking for a Clinical Study Build Programmer responsible for programming and testing clinical trial data collection databases.Key Responsibilities : Program and test data collection systems and mappings for clinical trialsEnsure accurate and efficient delivery of data collection systems aligned with study objectivesLead complex cross-functional projects and support regulatory activitiesRequired Qualifications : Master's degree with 5 years of experience in database programming or system validation, or Bachelor's degree with 7+ years of experienceKnowledge of regulatory guidelines such as GCP and 21 CFR Part 11Experience with clinical technologies including CTMS and EDCMinimum 4 years' oncology experience preferredProject and vendor management experience