Analytical Monitor (Central Review Lead – Clinical Data Analytics)
Location: India (Bangalore, Chennai, Trivandrum)
Job Type: Full-Time | Office with Flex
Company: ICON plc
Job ID: JR144388
About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is hiring an Analytical Monitor (Central Review Lead) to join its Integrated Data Analytics & Reporting team. This role is critical in enabling proactive, data-driven risk identification at site and subject levels to ensure clinical trial quality, patient safety, and operational efficiency.
You will work across multiple mid-to-high complexity studies, delivering analytical insights, supporting risk-based monitoring strategies, and collaborating with global cross-functional teams.
Key Responsibilities
Perform analytical monitoring to identify site- and subject-level risks, trends, and data quality issues
Conduct regular data reviews to detect early warning signals and prevent recurrence of issues
Analyze clinical data from multiple systems, platforms, and reporting tools to generate actionable insights
Collaborate with Site Management, Central Monitoring, and Data Management teams for risk-based decision-making
Support site prioritization and risk mitigation strategies through data-driven recommendations
Ensure compliance with SOPs, ICH-GCP guidelines, and regulatory requirements
Manage multiple workstreams and escalate risks or issues appropriately
Mentor and guide junior Analytical Monitors to enhance team capabilities
Required Qualifications & Experience
Bachelor’s degree in Health Sciences, Data Sciences, or a related field (Master’s preferred)
Minimum 4+ years of experience in pharmaceutical, biotech, or CRO industry
Strong understanding of clinical trial operations, data flow, and study execution
Proven experience in clinical data analysis and risk-based monitoring
Knowledge of statistical concepts and data interpretation
Experience in project management, risk management, and issue resolution
Familiarity with clinical data systems and analytics platforms
Excellent communication and cross-functional collaboration skills
Strong organizational and multitasking abilities in a fast-paced environment
Preferred Skills
Experience in central monitoring or advanced analytics roles
Exposure to global clinical trials and multi-study environments
Mentorship or team leadership experience
Why Join ICON
ICON provides an innovation-driven environment where data analytics and clinical research combine to improve trial outcomes and patient safety.
Key Benefits Include
Competitive salary and career advancement opportunities
Flexible work environment (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 a diverse and 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 development.
This role is ideal for experienced clinical data professionals seeking to advance their career in central monitoring, clinical analytics, and risk-based trial management within a leading global CRO.
Uttar Pradesh :
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Siliguri |Illinois :
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China | Quarry Bay |Liaoning :
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Peru | Argentina |Brazil :
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Tallinn |Hà Nội :
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