Full Time
Clinical Data Science Programmer
ICON PLC
Bangalore, Chennai, Trivandrum
Competitive
Posted 30/12/2025
About the Role
About Role & Responsibilities
• Review central lab and imaging data
• Support data analytics and reporting
• Maintain quality control of trial data
• Coordinate with global study teams
• Ensure protocol and regulatory compliance
Qualification
B.Pharm / M.Pharm / Pharm.D
Experience
1 – 4 years
Skills
• Clinical data management
• Centralized monitoring
• Regulatory documentation
• Reporting tools & analytics
About the Company
ICON is a leading global CRO delivering high-quality clinical research services worldwide
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