Integrated Study Timeline Implementation Manager

ICON Clinical Research, LP

Not specified; not specified; competitive salary w...
Microsoft project msp experience
Clinical study management oversight
Global regulatory compliance knowledge
This role involves leading the development and customization of Integrated Study Timelines for clinical trials in close collaboration with Global Trial Leads

Job Summary

  • This role involves leading the development and customization of Integrated Study Timelines for clinical trials in close collaboration with Global Trial Leads.
  • The successful candidate will possess over three years of Microsoft Project experience and five years of pharmaceutical industry experience including clinical study management.
  • 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 leading the development and customization of Integrated Study Timelines for clinical trials in close collaboration with Global Trial Leads.

Salary

Not specified; Not specified; Competitive salary with range of additional benefits including health insurance and retirement planning

Skills & Requirements

Must-have

  • Microsoft Project MSP experience
  • Clinical study management oversight
  • Global regulatory compliance knowledge
  • Timeline development and maintenance
  • Cross-functional stakeholder collaboration

Nice-to-have

  • Early phase or Phase 2/3 study experience
  • Multiple therapeutic area exposure
  • SharePoint user and document management
  • Excellent negotiation and facilitation skills
  • Process improvement initiative support

Key Requirements

  • Bachelor's degree required
  • 5+ years pharmaceutical/clinical research experience
  • 3+ years clinical study management/oversight
  • 3+ years Microsoft Project tool usage
  • Fluent business English proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter