Lead Clinical Research Associate

ICON Clinical Research, LP

United States Of America, United States
Oversee and manage clinical trial sites
Ensure compliance with regulatory requirements
Drive site performance
As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards

Job Summary

  • As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards.
  • You will be a key contributor to the success of clinical trials by driving site performance, providing mentorship to CRAs, and ensuring the highest levels of data quality and patient safety.
  • 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 Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards.

Skills & Requirements

Must-have

  • Oversee and manage clinical trial sites
  • Ensure compliance with regulatory requirements
  • Drive site performance
  • Ensure data quality and patient safety
  • Conduct source data verification

Nice-to-have

  • Foster an inclusive environment
  • Shape the future of clinical development
  • Support professional development of CRAs
  • Proactive approach to issue resolution

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Extensive experience as a Clinical Research Associate
  • Proven track record managing complex clinical trials
  • In-depth knowledge of ICH-GCP guidelines
  • Strong leadership and mentoring skills

Work Rights

Not specified

Tailored Resume

Cover Letter