Study Start Up Associate 2

ICON Broadbean

Turkey
Regulatory document preparation and submission
Liaising with internal and external stakeholders
Managing regulatory records
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.
  • 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 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 and submission
  • Liaising with internal and external stakeholders
  • Managing regulatory records
  • Process improvement initiatives

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Advancing innovative treatments and therapies
  • Nurturing talent

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Minimum 2 years experience in clinical research
  • Specific experience in study start-up activities
  • Understanding of ICH-GCP and local regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter