Hybrid Lab Data QC Specialist - LIMS

ICON; Ciudad de México; Híbrido; MXN 420.000 - 640.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Descripción de la vacante

ICON plc is seeking a Configuration & QC (C&Q) Specialist I to join our Mexico City team. This hybrid office role supports ICON Central Laboratories by configuring and amending the clinical trial database (LIMs) to ensure data integrity and project alignment.

You will assist project managers and setup specialists, perform QC checks on study data, and collaborate with cross-functional teams to resolve discrepancies and improve data reliability in clinical trials.

Formación

• Bachelor's degree in life sciences or related field.
• 1+ years of clinical data management, data entry, or laboratory experience, preferably in pharma/biotech.
• Familiarity with LIMS information management systems.
• Strong attention to detail and analytical skills.

Responsabilidades

• Assist ICL Project Managers and Setup Specialists in configuring and setting up the clinical trial laboratory database to ensure accuracy and alignment with project specifications.
• Perform quality control checks on the clinical trial database and study documentation to identify discrepancies and data-entry errors.
• Collaborate with cross-functional teams to address QC findings and ensure data integrity and reliability in clinical trials.

Conocimientos

Clinical data management

Quality control

Data entry

LIMS familiarity

Team collaboration

Educación

Bachelor's degree in life sciences

Herramientas

LIMS

Descripción del empleo

ICON plc is seeking a Configuration & QC (C&Q) Specialist I to join our Mexico City team. This hybrid office role supports ICON Central Laboratories by configuring and amending the clinical trial database (LIMs) to ensure data integrity and project alignment.

You will assist project managers and setup specialists, perform QC checks on study data, and collaborate with cross-functional teams to resolve discrepancies and improve data reliability in clinical trials.