Clinical Trial Associate 3 (cta 3)

ICON

Mexico City, Mexico
Not specified; competitive salary mentioned; vario...
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Bachelor's degree in life sciences or related field
Solid understanding of clinical trial processes
Strong knowledge of good clinical practice guidelines
** ICON is seeking a Clinical Trial Associate 3 in Mexico City to support the management and monitoring of clinical trial sites, ensuring compliance with protocols and regulations. The ideal candidate will possess relevant clinical research experience, strong organizational skills, and effective communication abilities. **

Job Summary

  • ICON plc is a world-leading healthcare intelligence organization fostering an inclusive environment for clinical development.
  • The role involves coordinating monitoring activities at clinical trial sites while ensuring adherence to study protocols and GCP guidelines.
  • Employees receive competitive benefits including health insurance, retirement planning, and access to a global Employee Assistance Programme.

Matching Summary

Match Score: 75

** ICON is seeking a Clinical Trial Associate 3 in Mexico City to support the management and monitoring of clinical trial sites, ensuring compliance with protocols and regulations. The ideal candidate will possess relevant clinical research experience, strong organizational skills, and effective communication abilities. **

Salary

Not specified; Competitive salary mentioned; Various annual leave entitlements and health insurance offered

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences or related field
  • Solid understanding of clinical trial processes
  • Strong knowledge of Good Clinical Practice guidelines
  • Experience in site management or clinical monitoring
  • Excellent analytical skills and attention to detail

Nice-to-have

  • Willingness to travel approximately 25%
  • Ability to mentor junior staff members
  • Cross-functional team collaboration experience
  • Proven project management capabilities

Key Requirements

  • Bachelor's degree in relevant field
  • Prior clinical research experience required
  • Understanding of regulatory requirements

Work Rights

Not specified

Tailored Resume

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