Data Integrity and Monitoring Specialist

Job Description: Data Monitoring & eCRF Design Specialist

Role Overview

The Data Monitoring & eCRF 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 eCRF 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 (eCRFs) 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 eCRF designs.
3. Perform ongoing data monitoring to ensure data accuracy, consistency...