Coding Specialist

New

IndiaFull-TimeMiddle

Salary not disclosed

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Job Details

Experience: 5–7 years

Requirements

5–7 years of experience in clinical data coding within clinical trials or pharmaceutical/CRO environments.
Strong knowledge of medical coding dictionaries such as MedDRA and WHODrug.
Experience using coding tools (e.g., Medidata Coder, Central Coding).
Solid understanding of the clinical trial process, clinical data management, and ICH-GCP guidelines.
Familiarity with thesaurus management and global coding standards.
Strong analytical skills.
Bachelor’s degree in life sciences, pharmacy, nursing, or a related healthcare field.
MedDRA certification is a strong advantage.

Responsibilities

Perform independent medical coding activities for assigned global clinical research projects.
Manage thesaurus and dictionary coding tasks using tools such as MedDRA and WHODrug.
Collaborate with clinical data management, safety, programming, and biostatistics teams.
Review and support Data Management Plans and study-specific coding conventions.
Identify and resolve coding-related issues.
Support the development and implementation of SOPs and global coding best practices.
Maintain technical expertise through continuous training.

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