Medical Coding Specialist
Job Summary
To support an ongoing clinical study, the full-time Medical Coding Specialist will perform accurate medical coding activities for clinical trial data using MedDRA, working remotely on a contract basis.
Key Responsibilities
- Perform manual coding of clinical trial data using MedDRA
- Code adverse events, medical history, and other study-related clinical data
- Maintain coding quality, consistency, and compliance with study requirements
Required Qualifications
- Previous experience in medical coding within a clinical research, biotech, pharmaceutical, or CRO environment
- Strong knowledge and practical experience working with MedDRA
- Experience performing manual coding of adverse events and medical history data
- Understanding of clinical trial processes and clinical data management principles
- Strong attention to detail and ability to work independently in a remote environment
Complete Job Description
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