Site Management Associate Ii

ICON plc

Buenos Aires, Argentina
Not specified; competitive salary mentioned; range...
Hybrid
Bachelor's degree in health sciences
3 years clinical trial administration experience
Good clinical practice (gcp) guidelines knowledge
This role supports the management and monitoring of clinical trial sites by ensuring compliance with study protocols and GCP guidelines

Job Summary

  • This role supports the management and monitoring of clinical trial sites by ensuring compliance with study protocols and GCP guidelines.
  • The successful candidate will lead the development of Investigator Site Files, manage payment services, and support audit readiness activities.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.

Matching Summary

This role supports the management and monitoring of clinical trial sites by ensuring compliance with study protocols and GCP guidelines.

Salary

Not specified; Competitive salary mentioned; Range of additional benefits offered

Skills & Requirements

Must-have

  • Bachelor's degree in health sciences
  • 3 years clinical trial administration experience
  • Good Clinical Practice (GCP) guidelines knowledge
  • Site Management Associate II role responsibilities

Nice-to-have

  • Leadership skills and development potential
  • Proactive and tech-savvy attitude
  • Attention to detail and organizational skills
  • Mentoring new hires and entry-level CTAs

Key Requirements

  • Bachelor's degree in health sciences or administrative programs
  • At least 3 years relevant experience in clinical trial administration
  • Advanced English language proficiency
  • Office-based work requirement in Buenos Aires, Argentina

Work Rights

Must be eligible to work in Argentina

Tailored Resume

Cover Letter