Clinical Study Manager

ICON plc

Competitive salary; various annual leave entitleme...
Not specified
Medical device clinical study management
End-to-end study delivery ownership
Cro partner management experience
ICON plc is seeking a Clinical Study Manager to oversee medical device clinical studies in Africa, the Middle East, and India. The ideal candidate should have a strong background in clinical trial management, regulatory compliance, and project management, with a focus on medical devices

Job Summary

  • ICON plc is a world-leading healthcare intelligence organization seeking an experienced Clinical Study Manager to drive innovation in medical device clinical development.
  • The role involves leading the operational delivery of medical device studies across Africa, the Middle East, and India while ensuring quality, compliance, and timeline adherence.
  • Candidates will benefit from a competitive salary, diverse health insurance offerings, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

Match Score: 85

ICON plc is seeking a Clinical Study Manager to oversee medical device clinical studies in Africa, the Middle East, and India. The ideal candidate should have a strong background in clinical trial management, regulatory compliance, and project management, with a focus on medical devices.

Salary

Competitive salary; Various annual leave entitlements; Health insurance and retirement planning offerings

Skills & Requirements

Must-have

  • Medical device clinical study management
  • End-to-end study delivery ownership
  • CRO partner management experience
  • Protocol development and endpoint definition
  • Ethics committee submission expertise

Nice-to-have

  • Experience working across African regions
  • Strong interpersonal collaboration skills
  • Willingness to travel extensively
  • Detail-oriented organizational abilities

Key Requirements

  • Bachelor's degree in relevant field
  • Minimum 3 years clinical trial management experience
  • Prior experience as Clinical Research Associate
  • Proven medical device study management from start-up to close-out

Work Rights

Not specified

Tailored Resume

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