Senior Clinical Coding Specialist

🔥 5 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

🏥 Medical Billing and Coding

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead clinical coding activities across multiple studies, ensuring high-quality and timely delivery of coding outputs • Perform and oversee coding of adverse events, medical histories, medications, and other clinical terminology using industry-standard and sponsor-specific dictionaries • Support study start-up activities, including input into Data Management Plans, User Acceptance Testing, database specifications, and CRF reviews • Generate, review, and reconcile coding consistency reports to ensure data accuracy and compliance with study requirements • Coordinate dictionary implementation, maintenance, and version updates throughout the study lifecycle • Partner with sponsors, medical monitors, and cross-functional teams to resolve coding questions and provide coding-related guidance • Identify opportunities for process and technology improvements, implement enhancements, and monitor outcomes • Mentor and support junior coding staff while contributing to operational excellence and adherence to company SOPs • Provide coding metrics, project updates, and operational support to management, including backup support for Clinical Coding and Data Management leadership when required

🎯 Requirements

• Degree in Life Sciences, Nursing, or a related discipline, or equivalent relevant industry experience • Minimum of 3 years of experience in clinical data coding or a related role within the pharmaceutical, biotechnology, or medical device industry • Hands-on experience using industry-standard coding dictionaries such as MedDRA and WHO-DD • Strong understanding of clinical coding processes, dictionary maintenance, and coding quality standards • Experience supporting study start-up activities, coding reviews, reporting, and database-related testing activities • Excellent organizational skills with the ability to manage multiple priorities and deliver against study timelines • Strong interpersonal and communication skills with the ability to collaborate effectively in a global environment • Proficiency in English • Strong computer literacy • Exceptional attention to detail and data quality

🏖️ Benefits

• Collaborative and inclusive environment • Growth and career development opportunities • Opportunity to learn and grow • Mentoring opportunities and support for junior team members

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