Clinical Trial Submission Manager Associate

ICON Clinical Research, LP

Istanbul, Turkey
100% onsite
Fluent in turkey process
Proficiency in regulatory submission processes
Strong attention to detail
ICON Clinical Research is seeking a Clinical Trial Submission Manager Associate in Istanbul, Turkey. The role involves managing regulatory submissions and communications with ethics committees and regulatory authorities, requiring fluency in Turkey's processes and a background in regulatory affairs

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • As a Regulatory Affairs Specialist, you will play a pivotal role in designing and analyzing clinical trials.
  • ICON offers a range of additional benefits designed to be competitive within each country.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Clinical Trial Submission Manager Associate in Istanbul, Turkey. The role involves managing regulatory submissions and communications with ethics committees and regulatory authorities, requiring fluency in Turkey's processes and a background in regulatory affairs.

Skills & Requirements

Must-have

  • Fluent in Turkey process
  • Proficiency in regulatory submission processes
  • Strong attention to detail

Nice-to-have

  • Excellent communication skills
  • Diverse and dynamic team environment
  • Focus on well-being and work-life balance

Key Requirements

  • Bachelor's degree in a scientific field
  • 1-2 years of experience in regulatory affairs

Work Rights

Not specified

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