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 / Beneficiosopportunities for personal and professional growthcollaborative culturevalues-driven environmentflexibilityimpactful patient outcomes ResponsabilidadesManual coding of clinical trial data using MedDRACode adverse events (AEs), medical history (MH), and other study-related dataReview verbatim terms for correct dictionary assignmentMaintain coding quality, consistency,



and study complianceResolve coding queries and support data review/cleaningCollaborate with study teams to meet project timelines Requisitos principalesExperience in medical coding within clinical research, biotech, pharmaceutical, or CROStrong knowledge and practical MedDRA experienceExperience coding AEs and MH data manuallyUnderstanding of clinical trial processes and data management principlesStrong attention to detail and ability to work independently remotelyExcellent communication and organizational skillsAttention to detailIndependent work ethicClear communicationMedDRA proficiencyManual coding of AE and MH dataClinical data management understanding

📌 Medical Coding Specialist (Barcelona)
🏢 Jobrapido
📍 Barcelona