Study Start Up Specialist

ICON

Burlington, Canada
On-site
Regulatory start-up
Site identification
Country and site distribution
ICON is seeking a Study Start Up Specialist to join their inclusive team in Burlington, Canada. The role focuses on driving study initiation and ensuring regulatory compliance within clinical trials, requiring a candidate with a medical or science background and a minimum of three years of industry experience

Job Summary

  • As a Study Start Up Specialist at ICON, you will be working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and executing the plan for country and site distribution.
  • Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies, ensuring compliance with all necessary regulations and guidelines.
  • 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

Match Score: 85

ICON is seeking a Study Start Up Specialist to join their inclusive team in Burlington, Canada. The role focuses on driving study initiation and ensuring regulatory compliance within clinical trials, requiring a candidate with a medical or science background and a minimum of three years of industry experience.

Skills & Requirements

Must-have

  • Regulatory start-up
  • Site identification
  • Country and site distribution
  • Subject Information Sheets/Informed Consent Forms

Nice-to-have

  • Inclusive environment
  • Fast-paced environment
  • Patient safety standards

Key Requirements

  • 3 years of industry experience
  • Knowledge of study start-up requirements
  • Bachelor's degree or local equivalent

Work Rights

Not specified

Tailored Resume

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