Clinical Coding Manager

🔥 19 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

👔 Manager

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Serve as the medical coding subject matter expert, driving quality, consistency, efficiency, and continuous improvement across coding activities • Plan, direct, coordinate, and oversee clinical medical coding activities in alignment with company procedures, industry regulations, and applicable guidelines • Lead coding and dictionary-related initiatives supporting clinical development and regulatory activities • Manage medical coding dictionaries and synonym lists, including dictionary maintenance and version updates • Review coded clinical data for consistency, accuracy, quality, and compliance with coding guidelines • Prepare and provide coding reports for medical review and decision-making activities • Partner with cross-functional teams to support timely and accurate medical coding across clinical programs • Deliver training on medical coding processes, standards, and best practices • Monitor compliance with standard operating procedures and identify and address process gaps • Maintain and control organizational access to coding dictionary portals and related systems

🎯 Requirements

• Bachelor's Degree in Nursing, Biology, or a related field • 7 years of experience in a clinical coding role • Expert knowledge of clinical data coding methodologies and medical coding practices • Expert understanding of clinical research, clinical trial execution, and applicable regulatory requirements and guidelines, including ICH-GCP and safety reporting requirements • Expert knowledge of industry-standard coding dictionaries, including MedDRA and WHODrug • Strong written and verbal communication skills • Excellent analytical and problem-solving abilities • Deep attention to detail and ability to interpret and consistently apply medical coding guidelines • Experience working within clinical research and regulated environments • Ability to collaborate effectively with cross-functional stakeholders • Strong organizational and time management skills • Ability to manage multiple priorities independently • Experience working with medical coding dictionaries, coding processes, and clinical data standards

🏖️ Benefits

• Flexible work arrangements / remote capacity • Opportunities for professional growth • Opportunities to work across therapeutic areas • Opportunities to engage with strategic coding initiatives

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