Job Title: Senior Clinical Data Coordinator (Senior CDC)
Company: ICON Clinical Research
Location: Bangalore, India
Employment Type: Full-time
Work Mode: Office or Home (Hybrid/Flexible)
Department: Clinical Data Management
Experience Required: 5+ years of experience in Clinical Data Management (CDM), clinical trial data review, eCRF management, data reconciliation, and study-level data management activities.
Education: Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, Biotechnology, or a related field.
Salary Package: ₹10–18 LPA (Estimated as per current market standards for Senior Clinical Data Coordinator roles in India; final compensation depends on experience, EDC expertise, and interview performance.)
Key Responsibilities:
Support Data Management Study Leads in managing clinical data activities.
Maintain and review:
Electronic Case Report Forms (eCRFs)
Data Validation Specifications (DVS)
Study-specific procedures
Perform clinical data review and third-party data reconciliation.
Manage data queries and ensure timely resolution of data discrepancies.
Track study metrics and provide status updates to:
Clinical Data Scientists
Project Teams
Functional Management
Analyze data issues and recommend appropriate solutions.
Conduct root cause analysis to identify and resolve recurring data problems.
Ensure clinical data quality, accuracy, and compliance with study requirements.
Collaborate with cross-functional teams including Clinical Operations, Biostatistics, and Project Management.
Required Skills:
Clinical Data Management (CDM)
Clinical Trial Data Review
eCRF Development & Maintenance
Data Validation Specifications
Data Reconciliation
Query Management
Electronic Data Capture (EDC) Systems
Medidata Rave / Oracle RDC / Similar Platforms
ICH-GCP Guidelines
Regulatory Compliance
Data Quality Management
Root Cause Analysis
Clinical Trial Documentation
Microsoft Office Suite
Stakeholder Communication
Attention to Detail
Preferred Skills:
Experience managing global clinical trials.
Strong knowledge of pharmaceutical/CRO clinical research processes.
Experience working with EDC and clinical data management systems.
Ability to handle complex data issues independently.
Strong analytical and problem-solving skills.
Experience supporting study timelines and deliverables.
Work Location: Bangalore, India
Benefits:
Competitive salary and performance incentives.
Health and wellness benefits.
Medical, insurance, and retirement plans (as applicable).
Learning and development opportunities.
Career growth pathways within clinical research.
Opportunity to work on global clinical development programs.
Collaborative and inclusive work environment.
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