Study Start Up Associate Ii (providing Support To North America)

ICON

Multiple Locations
Fully remote
Clinical trial start-up activities
Regulatory document preparation
Investigator site 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 innovative 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 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 the company is committed to providing a workplace free of discrimination and harassment.

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 innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial start-up activities
  • regulatory document preparation
  • investigator site coordination
  • ICH-GCP compliance
  • project management skills
  • cross-functional team collaboration

Nice-to-have

  • process improvement initiatives
  • strong communication skills
  • experience working with US sites
  • multinational study support

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter