Project Manager, Feasibility Site Activation

ICON plc

Poland
Not specified; benefits: competitive within countr...
Fully remote
Proven study start-up experience
Global multi-country clinical studies
Regulatory and ethics submission processes
This role is critical for driving the successful start-up of global clinical studies by taking ownership of Study Start-Up strategy and execution

Job Summary

  • This role is critical for driving the successful start-up of global clinical studies by taking ownership of Study Start-Up strategy and execution.
  • The position involves leading end-to-end start-up activities from site identification through IP release while ensuring high-quality, compliant approvals across regions.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture dedicated to inclusion and belonging.

Matching Summary

This role is critical for driving the successful start-up of global clinical studies by taking ownership of Study Start-Up strategy and execution.

Salary

Not specified; Benefits: Competitive within country; Additional: Health insurance, retirement planning, EAP

Skills & Requirements

Must-have

  • Proven Study Start-Up experience
  • Global multi-country clinical studies
  • Regulatory and ethics submission processes
  • Site contract and budget negotiations
  • CTMS and eTMF system familiarity
  • ICH-GCP regulatory framework knowledge

Nice-to-have

  • Cross-functional global team collaboration
  • Strategic input at Bid Defence meetings
  • Process consistency and continuous improvement
  • Strong stakeholder management skills
  • Solution-oriented approach to delivery

Key Requirements

  • Recent SSU primary responsibility experience
  • End-to-end site activation ownership
  • Experience with CA/EC and CTA strategy

Work Rights

Not specified

Tailored Resume

Cover Letter