Clinical Study Specialist

ICON plc

Warren, NJ, USA
Hybrid
Experience supporting global trials
Tmf and ctms experience
Strong written and verbal communication
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • The role involves organizing reports, coordinating meetings, and contributing to study document reviews.
  • ICON fosters an inclusive environment and offers competitive benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • Experience supporting global trials
  • TMF and CTMS experience
  • Strong written and verbal communication

Nice-to-have

  • Vendor management experience
  • Self-starter with solution-oriented mindset
  • Experience in ICF review

Key Requirements

  • Bachelor's Degree
  • Minimum of 2 years industry experience
  • Experience in clinical trial management

Work Rights

Not specified

Tailored Resume

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