Medical Coding Specialist I – Clinical Data Coding (MedDRA/WHO Drug)
Location: India (Bangalore, Chennai, Trivandrum)
Job Type: Full-Time | Office or Home
Company: ICON plc
Job ID: JR145604
About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Medical Coding Specialist I to support clinical trial data accuracy and standardization. This role is essential in ensuring precise coding of medical data using global coding dictionaries, contributing to data integrity, regulatory compliance, and high-quality clinical outcomes.
You will collaborate with clinical and data management teams to classify medical terms, resolve discrepancies, and support consistent coding practices across multiple studies.
Key Responsibilities
Perform accurate coding of medical terms, adverse events, medications, and procedures using MedDRA and WHO Drug dictionaries
Ensure consistency and standardization of coding across clinical trials
Review and resolve coding discrepancies in collaboration with cross-functional teams
Provide guidance on coding conventions and best practices
Maintain up-to-date knowledge of medical coding standards and regulatory requirements
Contribute to process improvements and development of coding guidelines
Support audit readiness and ensure compliance with clinical data standards
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, or a related healthcare field
0–2 years of experience in medical coding, pharmacovigilance, or clinical data management (freshers with strong knowledge may be considered)
Knowledge of MedDRA and WHO Drug coding systems
Understanding of clinical trial processes and data workflows
Strong attention to detail and analytical thinking
Good communication and teamwork skills
Ability to work in a fast-paced, deadline-driven environment
Preferred Skills
Prior exposure to clinical databases or safety systems
Basic understanding of regulatory guidelines such as ICH-GCP
Experience working in global clinical research environments
Why Join ICON
ICON offers a collaborative and growth-focused environment, enabling professionals to build expertise in clinical research and data coding within global trials.
Key Benefits Include
Competitive salary and career development opportunities
Flexible work options (office or remote)
Generous leave policies
Comprehensive health insurance
Retirement and financial planning support
Global Employee Assistance Programme (24/7 well-being support)
Life insurance and wellness initiatives
Flexible, country-specific employee benefits
Diversity, Equity & Inclusion
ICON is committed to fostering an inclusive workplace and is an equal opportunity employer. All qualified applicants will be considered without discrimination.
Application Note
Candidates who may not meet every requirement are encouraged to apply. ICON values diverse talent and supports continuous learning and professional growth.
This role is ideal for entry-level to early-career professionals looking to build a career in medical coding, pharmacovigilance, and clinical data management within a leading global CRO.
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