Clinical Data Manager II- QC Specialist

Company: Cytel
The QC Specialist is responsible for planning, executing, and documenting Testing activities for EDC and other systems. This role ensures that systems are tested and programmed to specification, supporting regulatory requirements and high-quality clinical trial data collection. The QC Specialist works closely with Data Management, Database Development, and external partners to verify that system builds meet specification expectations prior to study deployment. and programmed to specification, supporting regulatory requirements and high-quality clinical trial data collection, and external partners to verify that system builds meet specification expectations prior to study deployment.
Originally posted on Himalayas