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ICON plc
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Senior CDC/CDC II Professional

Senior CDC/CDC II Professional

ICON plc

3 - 6 years

4 - 7 Lacs

chennai bengaluru thiruvananthapuram

Posted:1 week ago| Platform:

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Skills Required

assurance data management coding gcp pharma clinical trials clinical research healthcare oracle clinical data management

Work Mode

Work from Office

Job Type

Full Time

Job Description

We are currently seeking a Senior Clinical Data Coordinator to join our diverse and dynamic 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 inNvative treatments and therapies.

What you will be doing

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, to develop and execute data management strategies tailored to specific studies.

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.).

Mentor junior data coordinators, providing expert guidance on data reconciliation, coding, and cleaning procedures.

Your profile

Bachelors degree in a relevant field, such as Life Sciences or Healthcare.

Proven experience in clinical data management within the pharmaceutical or biotechNlogy 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.

KNwledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

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