Study Start Up Associate Ii

ICON Clinical Research, LP

Multiple Locations
Fully remote
Study start-up activities
Investigator initiation package compilation
Regulatory document submission
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.
  • You will be responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Sponsor standards.
  • 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 innovative treatments and therapies.

Skills & Requirements

Must-have

  • Study start-up activities
  • Investigator Initiation Package compilation
  • Regulatory document submission
  • ICH-GCP compliance
  • Site compliance tracking

Nice-to-have

  • Process improvement initiatives
  • Cross-functional team collaboration
  • Fostering inclusive environment
  • Advancing innovative treatments

Key Requirements

  • Minimum 2 years experience
  • Bachelor's degree in life sciences
  • Experience with US regulatory requirements
  • Proficiency in English language

Work Rights

Not specified

Tailored Resume

Cover Letter