ICON Plc, a global leader in healthcare intelligence, clinical research, medical coding, data management, and clinical operations, has opened 5 major job positions across India. These roles offer exceptional opportunities for life science graduates and experienced professionals aiming to build careers in clinical research, medical coding, clinical data management, EDC systems, and statistical programming.
If you’re looking for high-growth roles in the Indian clinical research industry, this is one of the best opportunities to apply.
🔹 1. Medical Coding Specialist II – Bangalore, Trivandrum, Chennai
Key Responsibilities
- Perform advanced medical coding using MedDRA and WHO Drug
- Ensure coding accuracy, regulatory compliance, and consistency
- Collaborate with clinical & data management teams
- Resolve coding discrepancies and support coding conventions
Qualifications
- Bachelor’s in Life Sciences/Healthcare
- Experience with MedDRA, WHO Drug
- Understanding of clinical trial processes and regulatory requirements
- Excellent problem-solving and communication skills
🔹 2. Senior CDC – Bangalore, Trivandrum, Chennai
Key Responsibilities
- Support Data Management Study Lead in eCRF and validation
- Manage data reconciliation and edit specifications
- Track study metrics and ensure data quality
- Resolve data-related issues and identify root causes
Qualifications
- Bachelor’s in Life Sciences
- 6+ years in clinical data management
- Knowledge of Medidata, Oracle RDC, or similar systems
- Familiarity with ICH-GCP
🔹 3. Configuration & QC Specialist I – Chennai
Key Responsibilities
- Assist in EDC system configuration (Medidata Rave, Oracle Clinical)
- Perform QC checks on clinical data
- Collaborate with data management and Biostats teams
- Support validation plans and system testing
- Conduct end-user training
Qualifications
- Bachelor’s in Life Sciences or Computer Science
- 1+ years in clinical data management/EDC
- Analytical and detail-oriented
🔹 4. Clinical Trial Manager – India (Remote)
Key Responsibilities
- Plan and manage clinical trials end-to-end
- Oversee timelines, budgets, vendor selection, and risk management
- Collaborate with trial investigators & global teams
- Ensure compliance with ethical & regulatory guidelines
Qualifications
- Degree in Medicine, Science, or equivalent
- Subject matter expertise in a therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
🔹 5. Senior Clinical Data Science Programmer – Chennai
Key Responsibilities
- Develop and validate programming solutions (SAS, R, Python)
- Support analysis & reporting for clinical trials
- Generate datasets, TLFs for regulatory submissions
- Guide on coding standards and QC measures
Qualifications
- Master’s in Computer Science, Life Sciences, or Statistics
- Strong experience in SAS/R/Python for clinical trials
- Excellent problem-solving and teamwork
⭐ Benefits Offered by ICON Plc
- Competitive salary
- Annual leave benefits
- Global Employee Assistance Program (TELUS Health)
- Health insurance plans for family
- Retirement planning programs
- Flexible benefits (gym, transport, childcare, health assessments)
- Inclusive and diverse work culture
📝 How to Apply
Application Link for Medical Coding Specialist II
Application Link for Senior CDC
Application Link for Configuration & QC Specialist I
Application Link for Clinical Trial Manager
Application Link for Senior Clinical Data Science Programmer
