CDC II
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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

What You Will Do:

Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:
- Review clinical data in various database formats, datasets, listings, reports, visualizations, and analytics for completeness, accuracy, and integrity.
- Raise, review and close of queries with EDC/CDMS ensuring that data is reviewed and corrected as required by qualified site staff.




- Working closely with the DM trial partners and provide support as required to additional Data Management activities.
- Follow the Data Management Monitoring (DMM) and Risk Assessment Categorisation Tool (RACT) on a trial.
- Planning, coordinating, and assessing the associated risks of data review using various tools and technologies.
- Support the creation and execution of data review related reports and data review strategy.
- Maintaining an overview of the data review status and communicating relevant information to the DM Trial Partners.
- Maintaining an overview of the data review status and communicating relevant information to the DM Trial Partners.
- Collaborating with relevant Trial Partners and other stakeholders to successfully achieve the data review deliverables on the trial.
- The CDIA may assume the Clinical Trial Data Manager (CTDM) role for the clinical trial(s).

Effectively communicate data findings including visualizations with clear explanations.
- Proactively own and indepen

📌 Cdc II (Bengaluru)
🏢 IRE
📍 Bengaluru