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Senior Medical Coding Specialist

Job not on LinkedIn

đŸ”„ 4 minutes ago

🌐 United Kingdom, Poland, +1 more countries – Remote

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⏰ Full Time

🟠 Senior

đŸ„ Medical Billing and Coding

đŸ‘» Ghost score 10%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

đŸ’Œ Consulting

đŸ„ Healthcare

📩 Logistics

Consulting ‱ Healthcare ‱ Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

‱ Ensure accurate and consistent coding of medical data for clinical trials ‱ Take ownership of scientific operations deliverables, applying expertise to complex challenges ‱ Independently review data coded by third parties to ensure consistent coding ‱ Oversee outsourced CRO work through medical coding review and synonym dictionary review ‱ Review and maintain guidance and training documentation for coding guidelines in accordance with ICH guidelines and dictionary definitions ‱ Support other departments concerning dictionary use and coding quality ‱ Collaborate on creation and maintenance of CDM documents referencing coding-related activities ‱ Support and manage MedDRA and WHO Drug Dictionary upversion activities, including third-party vendor-operated studies ‱ Ensure compliance with industry quality standards, regulations, guidelines and procedures

🎯 Requirements

‱ A degree in nursing, biology or health-related field ‱ English fluency ‱ 5+ years medical coding using MedDRA and WHO Drug Dictionaries ‱ 5+ years in Pharmaceutical/Biotechnology industry or CRO environment ‱ Knowledge of ICH/GCP guidelines and methodology ‱ Excellent verbal and written communication skills ‱ Detail oriented, ability to multitask with strong prioritization, planning and organization skills ‱ Excellent team player ‱ Proficiency in Microsoft Office Applications ‱ Working knowledge of MedDRA and WHO Drug best practice documents ‱ Experience with coding application(s), Veeva and Medidata RAVE Coder desirable ‱ Experience with data warehouse tools (ie. Elluminate, CORE) ‱ Good understanding of Clinical Data Management processes and the applicable regulatory requirements ‱ Legal right to work in the country where the role is based

đŸ–ïž Benefits

‱ Competitive base salary and performance related incentives ‱ Health and wellbeing programmes including medical, dental, and vision coverage where applicable ‱ Retirement and pension plans ‱ Life assurance and disability coverage ‱ Employee assistance programmes and wellbeing resources ‱ Learning and development opportunities through structured training and career pathways

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