Clinical Data Quality Associate

ICON plc

Mexico City, Mexico
Hybrid
Conduct quality control checks
Identify and resolve data discrepancies
Data review and validation activities
As a Clinical Data Quality Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Data Quality Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • Conduct quality control checks on clinical trial data to ensure accuracy, completeness, and consistency, and collaborate with data management teams to identify and resolve data discrepancies and anomalies.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.

Matching Summary

As a Clinical Data Quality Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Conduct quality control checks
  • Identify and resolve data discrepancies
  • Data review and validation activities
  • Generate data quality reports
  • Fluency in English

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Contribute to advancing treatments
  • Work effectively in a team

Key Requirements

  • Bachelor's degree or equivalent experience
  • Previous experience in data management or quality assurance
  • Familiarity with CDISC standards
  • Familiarity with FDA/EMA regulations
  • Familiarity with ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter