Study Start Up Associate 2

ICON plc

Turkey
Regulatory document preparation
Ethics committee submissions
Stakeholder coordination
As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of inNvative treatments and therapies

Job Summary

  • As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of inNvative treatments and therapies.
  • Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
  • 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.

Matching Summary

As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of inNvative treatments and therapies.

Skills & Requirements

Must-have

  • regulatory document preparation
  • ethics committee submissions
  • stakeholder coordination
  • record maintenance
  • ICH-GCP understanding

Nice-to-have

  • process improvement initiatives
  • foster an inclusive environment
  • drive innovation and excellence
  • advance innovative treatments

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 2 years experience
  • Specific experience in study start-up
  • Strong understanding of regulatory requirements
  • Excellent organizational skills
  • Excellent project management skills

Work Rights

Not specified

Tailored Resume

Cover Letter