Site Activation Partner (providing Support To North America)

ICON Clinical Research, LP

Mexico
Home-based - mexico
Study start-up activities
Regulatory document preparation
Stakeholder coordination
ICON Clinical Research is seeking a Study Start Up Associate II to facilitate the initiation of clinical trials in North America from a home-based position in Mexico. The ideal candidate will have a background in clinical research and regulatory affairs, with a focus on compliance and project management

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.
  • 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.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Study Start Up Associate II to facilitate the initiation of clinical trials in North America from a home-based position in Mexico. The ideal candidate will have a background in clinical research and regulatory affairs, with a focus on compliance and project management.

Skills & Requirements

Must-have

  • Study start-up activities
  • Regulatory document preparation
  • Stakeholder coordination
  • Record maintenance
  • ICH-GCP understanding

Nice-to-have

  • Process improvement initiatives
  • Cross-functional team collaboration
  • Inclusive environment fostering innovation

Key Requirements

  • Minimum of 2 years of experience
  • Bachelor's degree in life sciences
  • Experience with US process
  • Experience in study start-up activities

Work Rights

Required Exp. with US process

Tailored Resume

Cover Letter