Senior Clinical Data Coordinator (Senior CDC) – ICON
Location
Bangalore, India
Work Mode
Office or Home (Hybrid/Flexible)
Job Type
Full-time
Department
Clinical Data Management / Clinical Data Sciences
Experience Required
Relevant experience in Clinical Data Management (CDM) within:
Pharmaceutical industry
Biotechnology industry
Clinical Research Organization (CRO) environment
Experience supporting clinical trials, data review, reconciliation, and database activities preferred.
Estimated Salary Package (Market Standard)
₹12 – ₹22 LPA (approx.), depending on clinical data management experience, EDC expertise, therapeutic area exposure, and technical skills.
Job Overview
The Senior Clinical Data Coordinator (Senior CDC) at ICON supports high-quality clinical data management activities for global clinical trials. The role focuses on maintaining clinical databases, managing data reconciliation processes, tracking study metrics, resolving data issues, and ensuring accurate and compliant clinical trial data delivery.
The position requires collaboration with Data Management Leads, Clinical Data Scientists, project teams, and cross-functional stakeholders to support successful clinical study execution.
Key Responsibilities
Clinical Data Management Support
Assist Data Management Study Leads with:
Electronic Case Report Form (eCRF) maintenance
Data Validation Specifications (DVS)
Study-specific procedures
Support clinical database management activities.
Ensure data accuracy, completeness, and consistency throughout the study lifecycle.
Clinical Data Review & Reconciliation
Manage reconciliation activities for:
Clinical trial data
External/third-party data sources
Perform data review based on:
Edit specifications
Data review plans
Identify discrepancies and coordinate timely resolution.
Data Issue Management
Address clinical data-related queries and provide solutions.
Perform root cause analysis for data quality issues.
Support corrective and preventive actions for recurring issues.
Escalate critical data concerns to appropriate stakeholders.
Study Metrics & Reporting
Track study and task-related performance metrics.
Communicate status updates to:
Clinical Data Scientists
Project Teams
Functional Management
Support monitoring of timelines and operational deliverables.
Cross-Functional Collaboration
Work closely with:
Clinical Data Managers
Clinical Scientists
Biostatistics teams
Clinical Operations teams
Project Management teams
Participate in study meetings and data management discussions.
Support global clinical trial delivery.
Educational Qualification
Required:
Bachelor’s degree in relevant fields such as:
Life Sciences
Healthcare Sciences
Pharmacy
Biotechnology
Related disciplines
Required Skills
Strong understanding of clinical data management processes.
Experience working within pharmaceutical, biotechnology, or CRO environments.
Familiarity with clinical data management systems such as:
Medidata
Oracle RDC
Similar EDC platforms
Strong attention to detail and data quality focus.
Good analytical and problem-solving skills.
Ability to manage multiple tasks in a fast-paced environment.
Strong written and verbal communication skills.
Ability to collaborate with global teams.
Preferred Skills
Knowledge of:
ICH-GCP guidelines
Clinical trial regulations
Data quality standards
Clinical database processes
Experience with:
eCRF review
Query management
Data validation
External data reconciliation
Exposure to global Phase I–IV clinical trials.
Work Environment
Flexible office/home-based working model.
Collaboration with international clinical research teams.
Opportunity to support global drug development programs.
Who Should Apply
Senior Clinical Data Coordinators
Clinical Data Associates
Clinical Data Management Specialists
Junior Clinical Data Managers
Professionals with experience in clinical trial data management, EDC systems, data reconciliation, query resolution, and ICH-GCP-compliant processes looking to advance their career in global clinical research.
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