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Worldwide Clinical Trials

Contract research organization delivering clinical trials

Senior Clinical Coding Specialist

Clinical Research OperationsPosted on Nov 11
Full-timeNo salary listed

About the Job

Requirements

  • A degree in Life Sciences, Nursing, or a related discipline, or equivalent relevant industry experience.
  • At least 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.
  • A 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.
  • Proficiency in English and strong computer literacy.
  • Ability to manage multiple priorities and deliver against study timelines.
  • Ability to collaborate effectively in a global environment and maintain data quality and attention to detail.

Responsibilities

  • 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.

About the Company

Worldwide Clinical Trials

Contract research organization delivering clinical trials

Worldwide Clinical Trials is a contract research organization that provides drug development services for pharmaceutical and biotech companies, focusing on running clinical trials to bring new medicines to market. Its core work centers on the science and logistics of clinical trials—designing studies, coordinating sites and investigators, and managing data and regulatory processes to advance drug candidates through development. The company differentiates itself through its specialized, science-driven approach and global expansion achieved via strategic acquisitions, building a larger network and broader capabilities to support complex trial programs. After a history of ownership changes, including a re-launch in 2007 and a majority stake sale in 2023, the firm aims to grow further under new ownership while continuing to offer focused clinical trial services that support medical advancement.

Company size
1,001-5,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Morrisville, NC
Founded
1986

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