Overview 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 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)
🏢 Trial Form Support
📍 Barcelona