Clinical Data Coordinator II – Clinical Data Management
Location: Chennai, India
Job Type: Full-Time | Office with Flex
Company: ICON plc
Job ID: JR142313
Application Deadline: March 21, 2026
About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is hiring a Clinical Data Coordinator II to support clinical data management activities for global trials. This role is critical in ensuring high-quality clinical data through effective coordination, validation, and reconciliation processes.
You will work closely with data management leads and cross-functional teams to maintain data integrity, support study execution, and contribute to accurate clinical trial outcomes.
Key Responsibilities
Support the Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and study-specific procedures
Perform clinical and third-party data reconciliation based on edit checks and data review plans
Track and communicate study progress, data metrics, and task status to stakeholders
Address data-related queries and recommend effective solutions
Identify root causes of data discrepancies and implement corrective actions
Ensure data quality, consistency, and compliance throughout the study lifecycle
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Healthcare, or a related field
Minimum 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry
Intermediate knowledge of clinical data management processes and workflows
Experience with clinical data systems such as Medidata, Oracle RDC, or similar platforms
Strong attention to detail and ability to manage multiple priorities in a fast-paced environment
Excellent communication and collaboration skills
Preferred Skills
Knowledge of ICH-GCP guidelines and regulatory standards
Experience in global clinical trial data handling and reconciliation processes
Exposure to data validation and quality control practices
Why Join ICON
ICON offers a collaborative and growth-oriented environment where employees contribute to advancing clinical research and innovative therapies.
Key Benefits Include
Competitive salary and career development opportunities
Flexible work model (office with flexibility)
Generous leave policies
Comprehensive health insurance
Retirement and financial planning benefits
Global Employee Assistance Programme (24/7 support)
Life insurance and wellness programs
Flexible, country-specific employee benefits
Diversity, Equity & Inclusion
ICON is committed to fostering an inclusive workplace. All qualified applicants will receive equal consideration without discrimination.
Application Note
Candidates who may not meet all requirements are encouraged to apply. ICON values diverse experience and supports continuous professional growth.
This role is ideal for experienced clinical data professionals seeking to advance their career in clinical data management, data quality, and global trial execution within a leading CRO.
Uttar Pradesh :
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Tallinn |Hà Nội :
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