ICON plc is actively hiring for two entry-level clinical research roles in India: Clinical Data Coordinator I (CDC I) and Clinical Trial Associate (CTA). These roles are ideal for candidates from Life Sciences, Pharmacy, and Healthcare backgrounds looking to enter or grow in the clinical data management and clinical operations domain.
With locations in Bangalore, Chennai, and Trivandrum, and flexible work options, this is a strong opportunity to break into the global CRO ecosystem.
๐ Job Overview
1๏ธโฃ Clinical Data Coordinator I (CDC I)
Primary Focus: Clinical Data Management
Key Responsibilities:
- Support development of eCRF (Electronic Case Report Forms) and validation specs
- Perform clinical data review and discrepancy management
- Raise and track queries to investigator sites
- Collaborate with clinical data scientists & study teams
- Ensure compliance with ICH-GCP guidelines
- Manage study documentation, filing, and archiving
2๏ธโฃ Clinical Trial Associate (CTA)
Primary Focus: Clinical Trial Operations
Key Responsibilities:
- Assist in clinical trial coordination & administration
- Maintain Trial Master File (TMF) and regulatory documents
- Support preparation of ICFs and CRFs
- Track study milestones and ensure protocol compliance
- Coordinate with cross-functional stakeholders
๐ Qualifications (Both Roles)
Degrees: B.Pharm, M.Pharm, B.Sc, M.Sc, Life Sciences, Healthcare
Required Skills:
- Basic understanding of clinical research processes
- Knowledge of ICH-GCP guidelines
- Familiarity with tools like Medidata, Oracle RDC (for CDC role)
- Strong attention to detail and documentation skills
- Effective communication & teamwork ability
๐ฐ Salary (Estimated)
- Clinical Data Coordinator I: โน3.5 โ โน6 LPA
- Clinical Trial Associate: โน3 โ โน5.5 LPA
(Based on Indian CRO market benchmarks for entry-level roles)
๐ Benefits at ICON
- Health insurance for employees & family
- Paid leaves and work-life balance programs
- Retirement & financial planning benefits
- Employee Assistance Program (TELUS Health)
- Flexible benefits (gym, childcare, travel support)
- Inclusive and global work culture
๐ Job Locations
- Bangalore
- Chennai
- Trivandrum
- Remote/Hybrid flexibility available
๐ Why This Role Matters
These roles sit at the core of clinical trial execution and data integrity, making them critical for:
- Drug development lifecycle
- Regulatory submissions
- Patient safety and data accuracy
If you’re targeting careers in:
- Clinical Data Management
- Clinical Operations
- CRO Industry
๐ This is a highly strategic entry point.
๐ฅ How to Apply
