Study Start Up Associate

ICON Clinical Research, LP

Burlington, Canada
Fully remote
Regulatory document preparation
Stakeholder coordination
Record maintenance
As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating 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 I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
  • Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
  • In addition to your competitive salary, 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 I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • regulatory document preparation
  • stakeholder coordination
  • record maintenance
  • study document support
  • meeting participation

Nice-to-have

  • inclusive environment
  • fosters innovation
  • rewards high performance
  • nurtures talent
  • work life balance

Key Requirements

  • Bachelor's degree in life sciences
  • Previous experience preferred but not required
  • Strong attention to detail
  • Organizational skills
  • Excellent communication skills
  • Ability to work independently

Work Rights

Not specified

Tailored Resume

Cover Letter