CDC II/ Sr CDC

About the role

As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What you'll do

• Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders
• Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures
• Manage clinical and third-party data reconciliation based on edit specifications and data review plans
• Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management
• Address data related questions and recommend potential solutions

What you need

• Clinical data management
• Clinical research
• Learning and development
• Reconciliation
• Communication
• Any graduate