EDC Programmer

Role: EDC Programmer responsible for designing, developing, validating, and maintaining electronic data capture systems (Medidata Rave and Zelta) to support clinical trials in bladder cancer. Objectives: ensure high-quality, compliant, and efficient data collection aligned with protocols, standards, and regulatory requirements. Responsibilities: build and validate databases, develop edit checks and custom functions, support database lock and data cleaning, oversee user access and security, and collaborate cross-functionally with Data Management, Biostatistics, and Clinical Operations. Qualifications: Bachelor's or Master’s in Computer Science, Life Sciences, or related field; 5+ years of EDC programming experience, with hands-on expertise in Medidata Rave and Zelta platforms; strong understanding of clinical trial processes, data standards (CDISC/SDTM), and validation/UAT support. Preferred: prior CRO/vendor collaboration experience. HighValue: biologics or small molecule clinical trials, supporting data integrity and compliance, with a focus on GCP, 21 CFR Part 11, and inspection readiness. WorkSetup: Fully remote; no travel specified.