Clinical Study Lead

ICON Clinical Research, LP

Multiple Locations
Vendor oversight for budget and timelines
Study protocol understanding and sharing
Site readiness coordination
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
  • Responsibilities include vendor oversight, study protocol understanding, site readiness coordination, and financial management of studies.
  • ICON offers competitive salaries, diverse benefits focused on well-being and work-life balance, and fosters an inclusive and accessible environment.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.

Skills & Requirements

Must-have

  • Vendor oversight for budget and timelines
  • Study protocol understanding and sharing
  • Site readiness coordination
  • Review monitoring reports and deliverables
  • eTMF/TMF compliance review
  • Financial management of studies

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Mentorship and guidance to junior staff
  • Risk management initiatives
  • Audit and inspection support

Key Requirements

  • Undergraduate degree in clinical, science, or health related field
  • Licensed health-care professional
  • 5 years of relevant experience
  • Minimum 3 years in clinical research
  • Management role experience
  • Fluent English and host country language

Work Rights

Not specified

Tailored Resume

Cover Letter