Clinical Site Associate

ICON Clinical Research, LP

Czech Republic
On-site hybrid
Support site management activities
Maintain up-to-date site information
Assist cras and project teams
ICON Clinical Research is seeking a Clinical Site Associate in the Czech Republic to support site management activities for clinical trials. The ideal candidate should have a background in life sciences or a related field, alongside relevant experience and strong organizational skills

Job Summary

  • As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.
  • You will contribute to scientific operations activities, taking responsibility for your deliverables and working collaboratively.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Clinical Site Associate in the Czech Republic to support site management activities for clinical trials. The ideal candidate should have a background in life sciences or a related field, alongside relevant experience and strong organizational skills.

Skills & Requirements

Must-have

  • support site management activities
  • maintain up-to-date site information
  • assist CRAs and project teams
  • collaborate with internal stakeholders
  • contribute to process improvement

Nice-to-have

  • customer-focused approach
  • adapt to changing priorities
  • sharing best practices

Key Requirements

  • Bachelor's degree or equivalent experience
  • Initial experience in clinical research
  • Strong organizational skills
  • High attention to detail
  • Proficiency with MS Office
  • Ability to work collaboratively
  • Willingness to travel approximately 10%

Work Rights

Not specified

Tailored Resume

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