Clinical Data Coder

Roles and Responsibilities :

• Code clinical trial data using MedDRA terminology to ensure accurate and consistent reporting.
• Review case report forms (CRFs) for completeness, accuracy, and compliance with regulatory requirements.
• Collaborate with project teams to resolve discrepancies or issues related to coding errors or missing data.
• Ensure timely submission of high-quality coded datasets for inclusion in clinical trial reports.

Job Requirements :

• 5-8 years of experience in medical coding, preferably in the pharmaceutical industry.
• Strong knowledge of MedDRA terminology and guidelines for coding clinical trials.
• Ability to work independently with minimal supervision while maintaining attention to detail and meeting deadlines.