CDC I
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring recent 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.

We are currently seeking CDC I / CDC II to join our diverse and agile team. 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.).

Your profile
- Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
- Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
- Strong attention to detail and the ability to work effectively in a fast-paced environment.
- Excellent communication skills and the ability to collaborate with cross-functional teams.
- Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits
ICON offers a competitive and

📌 Cdc I (Chennai)
🏢 IRE
📍 Chennai