Medical Coder

🔥 0 minutes ago

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

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⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Medical Billing and Coding

👻 Ghost score 10%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

💼 Consulting

🏥 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

• Encode terms reported as adverse events and medical history, as well as prior and concomitant medications, using industry accepted dictionaries such as MedDRA and WHOdrug • Deliver scientific operations work to a high standard while working closely with the team and stakeholders • Perform coding in accordance with departmental coding conventions and company SOPs • Generate queries for clarification of potentially discrepant data • Assist with data coding consistency reviews and SAE reconciliation as needed • Collaborate with medical monitors, Clinical and Data Management team members to ensure timely processing of coding according to project timelines • Use coding tools such as Medidata RAVE Coder, TMS, and Veeva • Assist in interdepartmental training of new staff as needed

🎯 Requirements

• Bachelors degree or related health science background • Commensurate experience will be considered in lieu of a 4 year degree • 2+ years industry experience in pharmacovigilance, clinical research, and/or clinical data management required • Experience with MedDRA and WHODD preferred • Working knowledge of medical terminology, clinical trials & coding is essential • Excellent written and oral skills • Demonstrated ability to work both independently and within cross functional teams • Strong attention to detail and a commitment to high quality work • Legal right to work in the country where the role is based

🏖️ 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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