Study Start Up Associate 2

ICON Clinical Research, LP

Turkey
Regulatory document preparation
Ethics committee submissions
Liaising with stakeholders
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
  • liaising with stakeholders
  • maintaining regulatory records
  • ICH-GCP guidelines

Nice-to-have

  • process improvement initiatives
  • fostering inclusive environment
  • driving innovation and excellence
  • advancing innovative treatments

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum 2 years experience
  • Study start-up activities experience
  • Local regulatory requirements knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter