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(Sr) Project Manager, Feasibility Site Activation

  • Manager
  • Remote
  • Full time
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About the role

ICON conducts clinical research to help bring medicines and treatments to patients. You will lead feasibility and site activation strategy and delivery for global clinical studies.

What you'll do

  • Develop study start-up plans covering regulatory, ethics, and contract activities
  • Drive start-up from site identification through investigational product release
  • Oversee regulatory and ethics submissions across study regions
  • Negotiate site contracts and budgets with legal, finance, and sponsors
  • Coordinate study start-up team members and monitor delivery
  • Maintain study documentation, metrics, budgets, and sponsor updates

Skills

Must have

  • Study start-up
  • Site activation
  • Clinical trial feasibility
  • Regulatory submissions
  • Ethics submissions
  • Site contract negotiation
  • Budget negotiation
  • Clinical trial management systems
  • Ich-gcp

Tools

  • Ctms
  • Etmf

Who it's for

Domain
clinical research

About ICON plc

ICON plc has 27 open roles in Bangalore, at ICON plc Bengaluru. See every ICON plc role.

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