Leading the design and delivery of clinical trial systems, the full-time Clinical Data Systems Lead will manage EDC, IRT, and ePRO builds, ensuring compliance and consistency across studies, while working remotely or onsite in New Jersey. Key responsibilities Lead the design, build, and delivery of clinical trial systems including EDC, IRT, and ePRO Develop and implement common data standards across clinical studies Track study build progress and ensure timely delivery using project management methodologies Required qualifications Bachelor's degree in Business, Management Information Systems, Computer Science, Life Sciences, or a related field 7+ years of hands-on technical study build experience in Medidata Rave EDC Expertise in clinical trial system implementation (EDC, IRT, ePRO) Knowledge of CDASH and SDTM standards Understanding of GCP, ICH Guidelines, and clinical regulatory compliance
Clinical Data Systems Lead • Springfield, Missouri, United States
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