Overview

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In this role, you will perform accurate medical coding of clinical trial data using MedDRA, supporting a sponsor-led study from a remote setting. You’ll focus on coding adverse events, medical history, and related data, ensuring consistency and data quality. You will collaborate with study teams to meet project timelines and resolve coding queries. This position offers growth within a values-driven, collaborative CRO environment that emphasizes quality and patient impact.

Compensaciones / Ventajas

- opportunities for personal and professional growth
- collaborative culture
- values-driven environment
- flexibility
- impactful patient outcomes

Responsabilidades

- Manual coding of clinical trial data using MedDRA
- Code adverse events (AEs), medical history (MH), and other study-related data




- Review verbatim terms for correct dictionary assignment
- Maintain coding quality, consistency, and study compliance
- Resolve coding queries and support data review/cleaning
- Collaborate with study teams to meet project timelines

Requisitos principales

- Experience in medical coding within clinical research, biotech, pharmaceutical, or CRO
- Strong knowledge and practical MedDRA experience
- Experience coding AEs xqziphu and MH data manually
- Understanding of clinical trial processes and data management principles
- Strong attention to detail and ability to work independently remotely
- Excellent communication and organizational skills

- Attention to detail
- Independent work ethic
- Clear communication
- MedDRA proficiency
- Manual coding of AE and MH data
- Clinical data management understanding

📌 Medical Coding Specialist - barcelona
🏢 Jobrapido
📍 Barcelona