Principal Cra

ICON

US
Fully remote
Clinical trial site management
Regulatory compliance monitoring
Site performance oversight
As a Principal 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 Principal 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.
  • ICON offers a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance options, retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

Matching Summary

As a Principal 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

  • Clinical trial site management
  • Regulatory compliance monitoring
  • Site performance oversight
  • Source data verification
  • Mentoring Clinical Research Associates
  • ICH-GCP guidelines knowledge

Nice-to-have

  • Cross-functional team collaboration
  • Strong leadership skills
  • Excellent communication skills
  • Proactive problem-solving
  • Inclusive work environment

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Advanced degree preferred
  • Extensive CRA experience in pharmaceutical, biotech, or CRO
  • Proven track record managing complex clinical trials
  • In-depth knowledge of ICH-GCP and regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter