Clinical Project Manager

ICON

Mexico City, Mexico
Not specified; competitive within country; range o...
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Site start-up and activation experience
End-to-end clinical trial management
Global cross-functional team leadership
** ICON is seeking a Clinical Project Manager in Mexico City, requiring strong experience in site activation and project management within the clinical research industry. The role involves overseeing clinical trials from site start-up to execution, managing cross-functional teams, and ensuring compliance with regulatory requirements. **

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation.
  • The Clinical Project Manager will oversee the end-to-end delivery of clinical trials from Site Start-Up through study execution across multiple regions including Canada and Latin America.
  • The company offers competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to inclusion and belonging.

Matching Summary

Match Score: 75

** ICON is seeking a Clinical Project Manager in Mexico City, requiring strong experience in site activation and project management within the clinical research industry. The role involves overseeing clinical trials from site start-up to execution, managing cross-functional teams, and ensuring compliance with regulatory requirements. **

Salary

Not specified; Competitive within country; Range of additional benefits included

Skills & Requirements

Must-have

  • Site start-up and activation experience
  • End-to-end clinical trial management
  • Global cross-functional team leadership
  • Study budget and contract management
  • Regulatory and feasibility process knowledge

Nice-to-have

  • High-performance collaborative environment
  • Proactive risk identification and mitigation
  • Strong negotiation and stakeholder skills
  • Fast-paced matrix environment adaptability

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Extensive experience in site activation and clinical trial start-up
  • Proven experience as Study Lead or CPM managing multi-country studies

Work Rights

Not specified

Tailored Resume

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