We are conducting an exclusive scheduled walk-in dive event on 7th August 2026 at ICON Trivandrum for multiple CDC opportunities supporting for various clients. Immediate interaction with hiring managers. Limited slots!
As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing.
- Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Review clinical and third-party data based on edit specifications and data review plans.
- Issue clear, accurate, and concise queries to investigational sites.
- As required, communicate effectively with peers, clinical data scientist and functional management.
- Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).