Study Start Up Associate Ii

ICON Clinical Research, LP

Sao Paulo, Brazil
On-site
Regulatory document preparation
Stakeholder coordination
Record maintenance
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.
  • In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are 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
  • stakeholder coordination
  • record maintenance
  • ICH-GCP understanding
  • local regulatory requirements

Nice-to-have

  • process improvement initiatives
  • foster an inclusive environment
  • drive innovation and excellence

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 2 years of experience
  • Specific experience in study start-up activities
  • Excellent organizational and project management skills
  • Excellent communication and interpersonal skills

Work Rights

Not specified

Tailored Resume

Cover Letter