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 / Incentivos 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