OVERVIEW The Medical Coder is responsible for centralized medical coding activities and serious adverse event (SAE) reconciliation, serving as the lead coding resource for assigned clinical trials. This role ensures the accuracy and compliance of coding practices, maintains Medical Coding Guidelines and SAE Plans, and supports the reconciliation of serious adverse events.

KEY TASKS & RESPONSIBILITIES

Design and maintain Medical Coding Guidelines and Serious Adverse Event reconciliation plans in collaboration with sponsors

Perform precise and consistent medical coding following coding guidelines and utilizing MedDRA and WHODrug dictionaries

Conduct reviews for coding accuracy and consistency reviews including the approval of coded terms and synonym lists

Perform serious adverse event reconciliation across clinical trial databases, safety systems and other relevant sources

Generate coding/SAE queries as necessary

Collaborate with safety, clinical, and data management teams to resolve discrepancies and ensure accurate representation of medical coding and safety information

Document coding decisions and justifications for clarity and auditability

Assist in maintenance activities for coding tools, including User Acceptance Testing (UAT) script creation and execution

Participate in the completion of MedDRA and WHODrug dictionary up versioning workflow activities in alignment with medical coding guidelines





Perform testing of coding tool and deployment of coding/SAE listings in elluminate

Ensure compliance with eClinical Solutions and industry quality standards, regulations, guidelines, and procedures

Other duties as assigned

Education & Experience

Bachelor s degree in relevant health science or professional qualification in a relevant scientific/technical discipline preferred

5+ years experience in the Pharmaceutical/Biotechnology industry with medical coding experience using WHODrug and MedDRA preferred

Knowledge of industry standards, ICH guidelines, and regulatory requirements for medical coding

Professional Skills

Solid knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology

Excellent verbal and written communication skills

Detail oriented, ability to multitask with strong prioritization, planning and organization skills

Proven ability to work both independently and in a team setting.

Technical Skills Proficiency in Microsoft Office Applications

Experience working on EDC systems. Medidata Rave Coder experience desirable

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Medical Coder (Bengaluru)
🏢 eClinical Solutions
📍 Bengaluru