Clinical Data Manager II- QC Specialist
IndiaFull-time2–5 yrsPosted yesterday
Mid-level pharma role at Iblyjb. Needs 2+ years and a B.Tech, B.E. or B.Sc.
About the role
This role ensures that systems are tested and programmed to specification, supporting regulatory requirements and high-quality clinical trial data collection.
What you'll do
- Responsible for planning, executing, and documenting Testing activities for EDC and other systems
- Lead and execute testing activities ensuring systems are tested and fit for intended use prior to production release
- Develop, review, and maintain test documentation, including test plans, test scripts, testing summary
- Design test scenarios to validate eCRF functionality, edit checks, integrations, data listings, data entry workflows, and reporting functionality
- Execute testing, document results, identify defects, and collaborate with database developers to resolve issues
What you need
- Clinical data management
- Communication
- Documentation
- Test cases
- SOP writing
- Regression testing
Good to have
- Internal audit