Senior Medical Coding Lead for Clinical Trials

ICON Clinical Research

México

Híbrido

MXN 900.000 - 1.100.000

Jornada completa

Hace 6 días
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Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements
Health insurance options
Retirement planning options
Global EAP/LifeWorks program
Life assurance
Country-specific benefits (varies)

Descripción de la vacante

ICON Strategic Solutions in Mexico seeks a Senior Medical Coding Specialist to lead coding for clinical trial data, ensuring accuracy and regulatory compliance across complex datasets. The role requires expertise in MedDRA and the WHO Drug Dictionary and involves mentoring junior coders and partnering with cross-functional teams.

You will stay current with coding standards and regulatory changes, contributing to SOP development and timely deliverables while supporting global trial activities in

Formación

  • Bachelor's degree in life sciences or related field.
  • Certification in medical coding or clinical data management is a plus.
  • Extensive experience in medical coding with MedDRA and WHO Drug Dictionary knowledge.
  • Strong understanding of clinical trial processes and regulatory guidelines for coding and data management.
  • Excellent attention to detail and ability to mentor others.

Responsabilidades

  • Lead the medical coding process for clinical trial data, ensuring accuracy and compliance.
  • Code medical terms using MedDRA and WHO Drug Dictionary; ensure data quality.
  • Collaborate with clinical data management, safety, and operations teams to resolve discrepancies.
  • Provide guidance and training to junior coding specialists.
  • Help develop coding guidelines, QC processes, and SOPs.

Conocimientos

MedDRA coding
WHO Drug Dictionary
CDMS
Leadership
Regulatory knowledge
Clinical trial processes
Data interpretation

Educación

Bachelor's degree in life sciences
Medical coding certification

Herramientas

CDMS
Coding software

Descripción del empleo

ICON Strategic Solutions in Mexico seeks a Senior Medical Coding Specialist to lead coding for clinical trial data, ensuring accuracy and regulatory compliance across complex datasets. The role requires expertise in MedDRA and the WHO Drug Dictionary and involves mentoring junior coders and partnering with cross-functional teams.

You will stay current with coding standards and regulatory changes, contributing to SOP development and timely deliverables while supporting global trial activities in

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