Data monitoring and ecrf designer

Job Description: Data Monitoring & e CRF Design Specialist
Role Overview
The Data Monitoring & e CRF Design Specialist will be responsible for designing, managing, and monitoring clinical trial data systems to ensure accuracy, completeness, and regulatory compliance. The role focuses on e CRF development, data validation, and ongoing data review, while supporting essential medical and regulatory documentation as required.
Key Responsibilities
Data Monitoring & Management
1. Design, develop, and maintain electronic Case Report Forms (e CRFs) using Zoho Database in alignment with study protocols, CRFs, and regulatory requirements.
2. Collaborate with clinical operations, investigators, and study teams to understand data collection needs and translate them into user-friendly and compliant e CRF designs.
3. Perform ongoing data monitoring to ensure data accuracy, consistency, completeness, and timeliness across clinical studies.
4. Conduct quality checks, query mana...