Study Start Up Associate I

ICON Clinical Research, LP

Mexico City, Mexico
Regulatory document preparation and submission
Clinical trial initiation
Ich-gcp and local regulatory requirements
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.
  • Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
  • 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

  • Regulatory document preparation and submission
  • Clinical trial initiation
  • ICH-GCP and local regulatory requirements
  • Stakeholder coordination and liaison

Nice-to-have

  • Process improvement initiatives
  • Fostering an inclusive environment
  • Nurturing talent and rewarding performance

Key Requirements

  • Minimum 2 years experience
  • Bachelor's degree in life sciences
  • Study start-up activities experience

Work Rights

Not specified

Tailored Resume

Cover Letter