Clinical Associate Specialist

hace 1 mes


Xico, México Icon Plc A tiempo completo
Role Overview

We are seeking a highly motivated and organized Study Coordinator to join our clinical trials team.

Your primary responsibility will be to support the project manager and clinical trial managers in ensuring the smooth conduct of clinical studies.

About Us

Icon Plc is a world-leading healthcare intelligence and clinical research organization, dedicated to advancing clinical development and improving patient outcomes.

Our team is passionate about delivering exceptional results, and we're committed to fostering an inclusive environment that encourages innovation and excellence.

Key Responsibilities
  • Assist project managers and clinical trial managers in tracking and maintaining study activities.
  • Maintain the Trial Master File (TMF) throughout the study.
  • Provide administrative support to ensure global inspection readiness.
Requirements

To succeed in this role, you will need:

  • Bachelor's degree in a scientific or medical discipline or equivalent experience.
  • An understanding of pharmaceutical industry processes and medical terminology.
  • Good written and verbal communication skills in English.
What We Offer

In addition to your competitive salary, you can expect:

  • A range of annual leave entitlements to support work-life balance.
  • Health insurance options tailored to suit your needs.
  • Competitive retirement planning to maximize savings and plan for the future.
  • The opportunity to work with a diverse and inclusive team.
Salary

$70,000 - $90,000 per annum, depending on location and experience.



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