Project Manager, Feasibility Site Activation

ICON Clinical Research, LP

Poland
Not specified; competitive within each country; va...
Fully remote
Proven study start-up experience
Global multi-country clinical studies
Regulatory and ethics submission processes
This role involves driving the successful start-up of global clinical studies by owning the Study Start-Up strategy and execution

Job Summary

  • This role involves driving the successful start-up of global clinical studies by owning the Study Start-Up strategy and execution.
  • The position requires leading end-to-end start-up activities from site identification through IP release while ensuring regulatory compliance across regions.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to an inclusive workplace culture.

Matching Summary

This role involves driving the successful start-up of global clinical studies by owning the Study Start-Up strategy and execution.

Salary

Not specified; Competitive within each country; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings

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
  • Risk identification and mitigation strategies
  • Structured solution-oriented approach

Key Requirements

  • Recent SSU ownership experience
  • Experience with CA/EC and CTA strategy
  • Hands-on familiarity with CTMS/eTMF
  • Strong stakeholder management skills

Work Rights

Not specified

Tailored Resume

Cover Letter