Project Manager, Fsa

ICON plc

China
Not specified; competitive within each country; ra...
Study start up plan execution
Regulatory and ethics submission management
Contract negotiation with sites
The role involves leading all study start-up activities from site identification to IP release while ensuring adherence to SOW and budget constraints

Job Summary

  • The role involves leading all study start-up activities from site identification to IP release while ensuring adherence to SOW and budget constraints.
  • Candidates must be accountable for preparing and coordinating submissions to regulatory bodies and ethics committees across assigned countries.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and well-being.

Matching Summary

The role involves leading all study start-up activities from site identification to IP release while ensuring adherence to SOW and budget constraints.

Salary

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

Skills & Requirements

Must-have

  • Study Start Up Plan execution
  • Regulatory and ethics submission management
  • Contract negotiation with sites
  • ICH GCP and country regulation knowledge
  • Clinical Trial Agreement process management

Nice-to-have

  • Process improvement mindset
  • Team mentorship and coaching skills
  • Strategic input at Kick-Off meetings
  • Cross-functional collaboration abilities

Key Requirements

  • Familiarity with ICH GCP and relevant country regulations
  • Experience with Clinical Trial Management Systems
  • Ability to manage study resources per SOW

Work Rights

Not specified

Tailored Resume

Cover Letter