Senior Medical Coding Specialist - Clinical Trials Lead

ICON

Ciudad de México

In loco

MXN 600.000 - 750.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Health insurance
Annual leaveEntitlements
Retirement planning

Descrizione del lavoro

ICON in Mexico is seeking a Senior Medical Coding Specialist to lead coding for clinical trial data, ensuring accuracy and regulatory compliance. You will work with MedDRA and WHO Drug Dictionary, collaborating with data management and safety teams and mentoring junior coders.

You will stay current with coding standards, contribute to SOPs, and help ensure data quality across global studies.

Competenze

  • Bachelor’s degree in life sciences, healthcare or related field.
  • Extensive experience in medical coding with MedDRA and WHO Drug Dictionary knowledge.
  • Strong understanding of regulatory requirements for coding and data management.

Mansioni

  • Lead the medical coding process for clinical trial data with accuracy and consistency.
  • Collaborate with clinical data management, safety and operations teams to resolve coding discrepancies.
  • Mentor junior coding specialists and ensure training on coding best practices.
  • Develop and implement coding guidelines, QC processes and SOPs.
  • Ensure timely completion of coding tasks to meet project timelines.
  • Stay updated on coding standards and regulatory changes.

Conoscenze

Medical coding
MedDRA
WHO Drug Dictionary
CDMS
Leadership
Mentoring
Regulatory knowledge
Attention to detail
Cross-functional collaboration

Formazione

Bachelor's degree in life sciences/healthcare
Medical coding certification

Strumenti

CDMS
Coding software

Descrizione del lavoro

ICON in Mexico is seeking a Senior Medical Coding Specialist to lead coding for clinical trial data, ensuring accuracy and regulatory compliance. You will work with MedDRA and WHO Drug Dictionary, collaborating with data management and safety teams and mentoring junior coders.

You will stay current with coding standards, contribute to SOPs, and help ensure data quality across global studies.

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