Medical Coding Specialist

🔥 0 minutes ago

🌐 United States, Spain, +2 more countries – Remote

🇺🇸 United States – Remote 🇪🇸 Spain – Remote 🇵🇱 Poland – Remote 🇸🇪 Sweden – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🏥 Medical Billing and Coding

👻 Ghost score 10%

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TFS HealthScience - Contract Research Organization

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2007

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.

📋 Description

• Perform manual coding of clinical trial data using MedDRA • Code adverse events, medical history, and other study-related clinical data • Review and assess verbatim terms to ensure accurate dictionary assignment • Maintain coding quality, consistency, and compliance with study requirements • Resolve coding queries • Support ongoing data review and cleaning activities • Collaborate with study teams to complete coding activities according to project timelines • Support an ongoing clinical study dedicated to one global pharmaceutical or biotechnology sponsor

🎯 Requirements

• 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 • Ability to work independently in a remote environment • Excellent communication and organizational skills

🏖️ Benefits

• Opportunities for personal and professional growth • Rewarding work environment • Collaborative team culture • Work supporting improvements in patients’ lives • Remote work arrangement • Full-time 1.0 FTE contract/freelance assignment • Minimum 4-month duration • Start date ASAP