This role leads clinical database programming activities and manages the administration of Rave URL activities including report administration and user roles
Job Summary
This role leads clinical database programming activities and manages the administration of Rave URL activities including report administration and user roles.
The specialist is responsible for developing study databases by programming forms and edit checks according to CRF and Edit Check Specifications.
Candidates must possess a Bachelor's degree and over 8 years of clinical database programming experience within the medical device or pharma industry.
Matching Summary
This role leads clinical database programming activities and manages the administration of Rave URL activities including report administration and user roles.
Skills & Requirements
Must-have
Medidata Rave super user expertise
Clinical database programming experience
CRF specification programming
Edit check development skills
Global library development
Nice-to-have
Experience with complex global trials
Knowledge of data reconciliation workflows
Familiarity with UAT processes
Key Requirements
Bachelor's Degree in technical or scientific discipline
8+ years of clinical database programming experience