Clinical Study Manager

ICON plc

Medical device clinical studies
Operational delivery
Cro partner management
Support the delivery of medical device clinical studies across Africa, the Middle East (including Israel), and India

Job Summary

  • Support the delivery of medical device clinical studies across Africa, the Middle East (including Israel), and India.
  • Take ownership of the operational delivery of medical device clinical studies, ensuring quality, compliance, and timelines are consistently achieved.
  • ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

Support the delivery of medical device clinical studies across Africa, the Middle East (including Israel), and India.

Skills & Requirements

Must-have

  • Medical device clinical studies
  • Operational delivery
  • CRO partner management
  • Regulatory compliance
  • Protocol development contribution

Nice-to-have

  • Cross-regional oversight
  • Inclusive and diverse culture
  • Work-life balance focus

Key Requirements

  • Minimum of 3 years of experience in clinical trial management
  • Prior experience as a Clinical Research Associate
  • Proven experience managing medical device clinical studies
  • Strong understanding of medical device regulatory requirements
  • Experience working across Africa and or India regions is highly desirable
  • Willingness and ability to travel extensively

Work Rights

Not specified

Tailored Resume

Cover Letter