Senior Clinical Data Coordinator

About the role

As a Senior CDC 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

• Lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement
• Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements
• Participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and enhance data quality throughout the study lifecycle
• Collaborate closely with cross-functional teams, including clinical operations and biostatistics
• Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation

What you need

• Clinical research
• Clinical data management
• Documentation
• Reconciliation
• Communication
• Any graduate

Good to have

• Two-wheeler