Senior CDC
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive workplace driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

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:
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.




Identify root cause to systematically resolve data issues.

Your Profile:
You will bring relevant clinical data management experience, along with the following qualifications and skills.

Required qualifications and experience:
Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
Intermediate 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 workplace.
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.

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance

📌 Senior Cdc Bengaluru
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📍 Bengaluru