Lead Clinical Research Associate

ICON plc

United States Of America, United States
Ophthalmology or gene therapy experience
Ich-gcp guidelines knowledge
Regulatory requirements knowledge
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

  • Ophthalmology or Gene Therapy experience
  • ICH-GCP guidelines knowledge
  • Regulatory requirements knowledge
  • Clinical trial processes knowledge
  • Site selection and initiation
  • Source data verification

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Mentoring CRAs and site staff
  • Proactive 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 trials
  • Strong leadership and mentoring skills

Work Rights

Not specified

Tailored Resume

Cover Letter