Clinical Trial Submission Manager Associate

ICON Clinical Research, LP

Istanbul, Turkey
Clinical trial submission processes
Regulatory affairs
Ec and ra notifications
As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Clinical trial submission processes
  • Regulatory Affairs
  • EC and RA notifications
  • Amendment submissions
  • Payment management to ECs

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Shaping the future of clinical development
  • Global employee assistance program

Key Requirements

  • 1-2 years of experience in regulatory affairs
  • Bachelor's degree in scientific or healthcare field
  • Proficiency in regulatory submission processes
  • Fluent in Turkey process

Work Rights

Not specified

Tailored Resume

Cover Letter