Clinical Study Builder
Job Summary
Working remotely in a permanent full-time capacity, the Clinical Study Builder will design and develop electronic case report forms (eCRFs) and associated data quality checks for medical research studies, collaborating closely with data management and statistical staff while ensuring compliance with regulatory requirements.
Key responsibilities
- Develop programming and configuration of Rave, Veeva, and Medrio CRFs based on protocol requirements
- Lead eCRF design and review meetings, providing user and technical support
- Collaborate with Lead Data Managers and vendor partners for testing and deployment, troubleshooting technical issues as needed
Required qualifications
- B.Sc. or M.Sc. in a related field of study
- Minimum of 2-4 years of Rave CDMS study build experience
- Certified Rave Study Builders preferred, with detailed knowledge of case report form design
- Understanding of the drug development process and applicable regulations, including Good Clinical Practices
- Highly organized with effective project planning and time management skills
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