Clinical Trial Specialist

ICON

US
Fully remote
Site management of clinical trials
Compliance with regulatory requirements
Clinical trial protocol adherence
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • The role involves overseeing day-to-day site management activities to ensure clinical trial sites meet regulatory and operational requirements while delivering high-quality data.
  • ICON offers a competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • site management of clinical trials
  • compliance with regulatory requirements
  • clinical trial protocol adherence
  • clinical operations collaboration
  • data collection and reporting
  • mentorship of junior staff

Nice-to-have

  • problem-solving and organizational skills
  • effective communication and interpersonal skills
  • fostering collaboration and process improvement
  • inclusive and diverse workplace culture

Key Requirements

  • Bachelor’s degree in life sciences or related field
  • Extensive experience in site management or clinical operations
  • Strong understanding of Good Clinical Practice (GCP)
  • Experience in clinical research industry

Work Rights

Not specified

Tailored Resume

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