Medical Coding Specialist

This is a fully remote position, open to applicants in United States, +3 more countries.

📋 Description

• Execute manual coding of clinical trial data utilizing MedDRA.

• Code adverse events, medical history, and other clinical data pertinent to the study.

• Review and evaluate verbatim terms to ensure precise dictionary assignment.

• Uphold coding quality, consistency, and adherence to study requirements.

• Address and resolve coding inquiries.

• Assist in ongoing data review and cleaning processes.

• Collaborate with study teams to finalize coding tasks in alignment with project timelines.

• Support a continuous clinical study dedicated to a single global pharmaceutical or biotechnology sponsor.

⛳️ Requirements

• Prior experience in medical coding within a clinical research, biotech, pharmaceutical, or CRO setting.

• Comprehensive knowledge and hands-on experience with MedDRA.

• Experience in manual coding of adverse events and medical history data.

• Familiarity with clinical trial processes and clinical data management principles.

• Exceptional attention to detail.

• Capability to work independently in a remote setting.

• Outstanding communication and organizational skills.

🏝️ Benefits

• Opportunities for personal and professional development.

• Rewarding work environment.

• Collaborative team culture.

• Work that contributes to improvements in patients’ lives.

• Remote work arrangement.

• Full-time 1.0 FTE contract/freelance assignment.

• Minimum duration of 4 months.

• Immediate start date available.