Job Title: Clinical Data Coordinator II (Senior)
Company: ICON Clinical Research
Locations: Chennai / Trivandrum / Bangalore, India
Employment Type: Full-time
Work Mode: Office or Home (Hybrid/Flexible)
Department: Clinical Data Management
Experience Required: 2–5 years of experience in Clinical Data Management (CDM), clinical trial data review, and handling eCRF, data validation, and reconciliation activities within pharmaceutical, biotechnology, or CRO environments.
Education: Bachelor's degree in Life Sciences, Healthcare, Pharmacy, Biotechnology, or a related field.
Salary Package: ₹6–12 LPA (Estimated as per current market standards for Clinical Data Coordinator II roles in India; final compensation depends on experience, technical skills, and interview performance.)
Key Responsibilities:
Support Data Management Study Leads in maintaining:
Electronic Case Report Forms (eCRFs)
Data Validation Specifications (DVS)
Study-specific procedures
Perform clinical data review and third-party data reconciliation activities.
Manage data discrepancies based on edit checks and data review plans.
Track and communicate study metrics and task status to:
Clinical Data Scientists
Project Teams
Functional Managers
Address clinical data-related queries and provide appropriate solutions.
Identify root causes of data issues and implement corrective actions.
Ensure accurate, timely, and high-quality clinical data delivery.
Collaborate with cross-functional clinical trial teams.
Required Skills:
Clinical Data Management (CDM)
eCRF Development & Maintenance
Data Review & Reconciliation
Data Validation Specifications
Clinical Trial Data Handling
Query Management
Root Cause Analysis
Clinical Database Management
ICH-GCP Guidelines
Regulatory Compliance
Medidata Rave / Oracle RDC / Similar EDC Systems
Microsoft Office Suite
Communication & Stakeholder Management
Attention to Detail
Preferred Skills:
Experience working with global clinical trials.
Knowledge of pharmaceutical or biotechnology clinical development processes.
Experience with Electronic Data Capture (EDC) systems.
Understanding of clinical trial documentation and workflows.
Ability to manage multiple priorities in a fast-paced environment.
Work Locations:
Chennai, India
Trivandrum, India
Bangalore, India
Benefits:
Competitive salary and performance incentives.
Health and wellness benefits.
Medical, insurance, and retirement benefits (as applicable).
Learning and development programs.
Structured career growth opportunities.
Opportunity to work on global clinical research programs.
Inclusive and collaborative work culture.
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