Clinical Study Manager

ICON

Kenya
On-site
End-to-end management of medical device clinical studies
Oversee study timelines, deliverables, and budgets
Manage cro partners
ICON is seeking a Clinical Study Manager in Kenya to oversee medical device clinical trials across Africa, the Middle East, and India. The ideal candidate will have strong project management skills and extensive experience in clinical trial management, particularly with medical devices

Job Summary

  • As a Clinical Trial Manager, you will support the delivery of medical device clinical studies across Africa, the Middle East (including Israel), and India.
  • As Clinical Study Manager, you will take ownership of the operational delivery of medical device clinical studies, ensuring quality, compliance, and timelines are consistently achieved.
  • In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Matching Summary

Match Score: 85

ICON is seeking a Clinical Study Manager in Kenya to oversee medical device clinical trials across Africa, the Middle East, and India. The ideal candidate will have strong project management skills and extensive experience in clinical trial management, particularly with medical devices.

Skills & Requirements

Must-have

  • end-to-end management of medical device clinical studies
  • oversee study timelines, deliverables, and budgets
  • manage CRO partners
  • ensure compliance with medical device regulations
  • manage submissions to ethics committees and regulatory bodies
  • provide regional oversight across Africa and India

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • work across diverse and growing regions

Key Requirements

  • minimum of 3 years of experience in clinical trial management
  • Prior experience as a Clinical Research Associate
  • demonstrated project management experience
  • 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