Job Title: Clinical Data Coordinator II (CDC II)
Company: ICON Clinical Research
Locations: Trivandrum / Bangalore / Chennai, 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, clinical trial data review, eCRF management, and data reconciliation activities within CRO, pharmaceutical, or biotechnology 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 expertise, 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 and third-party data reconciliation activities.
Review clinical trial data based on edit checks and data review plans.
Track and communicate study progress, metrics, and task status to:
Clinical Data Scientists
Project Teams
Functional Management
Address clinical data queries and recommend appropriate solutions.
Perform root cause analysis to identify and resolve data issues.
Ensure high-quality and timely delivery of clinical data management activities.
Collaborate with cross-functional teams involved in clinical trials.
Required Skills:
Clinical Data Management (CDM)
Clinical Trial Data Review
eCRF Management
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
Microsoft Office Suite
Communication & Collaboration Skills
Attention to Detail
Preferred Skills:
Experience working in pharmaceutical, biotechnology, or CRO environments.
Knowledge of clinical trial processes and regulatory requirements.
Experience with global clinical studies.
Ability to manage multiple tasks in a fast-paced environment.
Strong analytical and problem-solving ability.
Work Locations:
Trivandrum, India
Bangalore, India
Chennai, India
Benefits:
Competitive salary and performance incentives.
Health and wellness programs.
Medical, insurance, and retirement benefits (as applicable).
Employee assistance and wellbeing support.
Learning and development opportunities.
Structured career growth pathways.
Opportunity to contribute to global clinical research programs.
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