Senior Medical Coder

The Medical Coder plays a critical role in supporting clinical trials by ensuring the accurate, consistent, and timely coding of medical terms using standardized dictionaries (e.g., MedDRA, WHODrug). This individual brings advanced knowledge of medical terminology, clinical trial processes, regulatory requirements, and coding best practices. The Medical Coder collaborates cross-functionally with clinical operations, data management, safety and risk management, biostatistics, and medical writing teams to maintain high-quality data that meet global regulatory standards.
Proficient in Medidata RAVE and Coder.
Strong working knowledge of MedDRA and WHODrug dictionaries, including version control and update management.
Bachelor's degree in life sciences, nursing, pharmacy, public health, or equivalent healthcare background; advanced degree preferred.
2 years of medical coding experience in clinical research, ideally within CRO, pharmaceutical, or biotech environments.
Experience supporting multiple therapeutic areas; oncology, rare disease, or immunology experience preferred but not required.
Excellent understanding of ICH-GCP, FDA, EMA, and other global regulatory guidelines.
Strong attention to detail, analytical problem-solving, and ability to manage multiple projects simultaneously.
Effective communication skills and experience collaborating in matrixed research environments.

Skills
GCP, Risk Management, Clinical Research, Medical Writing

Work arrangement
Yes