Clinical Project Manager

ICON plc

Mexico City, Mexico
Not specified; competitive salary mentioned; range...
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Site start-up and activation experience
End-to-end clinical trial delivery
Global cross-functional team leadership
** ICON plc is seeking a Clinical Project Manager for a hybrid role based in Mexico City, responsible for overseeing the site activation process for clinical trials. The ideal candidate will possess extensive experience in site start-up, project management, and leading global teams within the clinical research industry. **

Job Summary

  • ICON plc is a world-leading healthcare intelligence organization seeking a Clinical Project Manager to drive clinical development innovation.
  • The role involves owning the end-to-end delivery of clinical trials from Site Start-Up through study execution across Canada and Latin America.
  • The company offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

Match Score: 75

** ICON plc is seeking a Clinical Project Manager for a hybrid role based in Mexico City, responsible for overseeing the site activation process for clinical trials. The ideal candidate will possess extensive experience in site start-up, project management, and leading global teams within the clinical research industry. **

Salary

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

Skills & Requirements

Must-have

  • Site start-up and activation experience
  • End-to-end clinical trial delivery
  • Global cross-functional team leadership
  • Study budget and contract management
  • Regulatory submission oversight

Nice-to-have

  • Strong negotiation and stakeholder skills
  • Proactive risk identification and mitigation
  • Experience in fast-paced matrix environment
  • Ability to foster high-performance culture

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Extensive experience in clinical trial start-up
  • Proven track record as Study Lead or CPM
  • Solid understanding of regulatory requirements

Work Rights

Not specified

Tailored Resume

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