Clinical Study Manager Ii

ICON Clinical Research, LP

Groningen, Netherlands
60% onsite
Clinical trial management
Cross-functional team leadership
Study plan development
As a Clinical Study Manager, you will play a central role in the planning, execution and oversight of (complex) clinical trials ensuring delivery to the highest standards of quality, compliance and collaboration

Job Summary

  • As a Clinical Study Manager, you will play a central role in the planning, execution and oversight of (complex) clinical trials ensuring delivery to the highest standards of quality, compliance and collaboration.
  • The Role In this role, you will gain deep exposure to Early Phase Clinical Research and support the CSM team across a broad range of study and population types, including patient research.
  • Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Matching Summary

As a Clinical Study Manager, you will play a central role in the planning, execution and oversight of (complex) clinical trials ensuring delivery to the highest standards of quality, compliance and collaboration.

Skills & Requirements

Must-have

  • Clinical trial management
  • Cross-functional team leadership
  • Study plan development
  • Risk analysis and mitigation
  • Operational challenge resolution

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Nurturing talent
  • Well-being and work-life balance

Key Requirements

  • MSc in Life Sciences or higher
  • Demonstrated project management experience
  • Clinical research experience
  • Strong people management skills
  • Fluent English and Dutch

Work Rights

Commutable distance to Groningen

Tailored Resume

Cover Letter