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Clinical Coder - Remote

Posted 1 week ago
All others
Full Time
USA

Overview

The Clinical Coder plays a crucial role in overseeing the coding process for clinical trials, ensuring data accuracy and compliance with regulatory standards.

In Short

  • Acts as Subject Matter Expert (SME) for coding tools and processes.
  • Reviews clinical trial data for completeness and accuracy.
  • Assigns codes to clinical trial data to comply with regulations.
  • Maintains records of coded data for compliance and audits.
  • Liaises with various teams for coding-related processes.
  • Participates in User Acceptance Testing for database builds.
  • Stays updated on coding regulations and industry best practices.
  • Conducts regular audits of coded data for quality assurance.
  • Ensures completion of study deliverables per timelines.
  • Performs additional duties as requested.

Requirements

  • Familiarity with clinical trial protocols and medical terminology.
  • Knowledge of coding processes and tools.
  • Technical knowledge in coding tool set-up and implementation.
  • Knowledge of safety management and event reporting.
  • Strong attention to detail and analytical skills.
  • Excellent teamwork and communication abilities.
  • Knowledge of clinical research regulatory requirements.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Effective time and financial management skills.
  • Ability to establish effective working relationships.

Benefits

  • Opportunity to work in a leading MedTech solutions company.
  • Collaborative and supportive team environment.
  • Engagement in impactful clinical trial services.
  • Continuous professional development and training.
  • Access to advanced technology platforms.
RQM+ logo

RQM+

RQM+ is a leading MedTech service provider with the largest global team of regulatory and quality experts, boasting over 40 years of regulatory expertise. The company offers a wide range of services including clinical trials, lab services, and reimbursement support, aimed at reducing risk and facilitating market access for medical devices, digital therapeutics, and diagnostics throughout their product lifecycle. RQM+ collaborates with 19 of the top 20 medical device manufacturers and seven of the top 10 in vitro diagnostic companies, leveraging a team with extensive experience from regulatory bodies such as the FDA and MHRA. Committed to employee development and work-life balance, RQM+ values its workforce as its greatest asset.

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