Clinical Research Associate Ii

ICON

Portugal
Clinical trial monitoring
Protocol compliance
Data integrity assurance
Clinical Research Associate II at ICON plays a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • Clinical Research Associate II at ICON plays a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a diverse culture that rewards high performance and nurtures talent, with benefits focused on well-being and work-life balance for employees and their families.
  • ICON is dedicated to providing an inclusive and accessible environment and is committed to equal employment opportunities without discrimination or harassment.

Matching Summary

Clinical Research Associate II at ICON plays a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial monitoring
  • protocol compliance
  • data integrity assurance
  • ICH-GCP guidelines knowledge
  • site qualification and initiation
  • patient safety management
  • travel up to 60%

Nice-to-have

  • strong organizational skills
  • effective communication skills
  • ability to work independently
  • collaborative team player
  • attention to detail
  • inclusive work environment

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years Clinical Research Associate experience
  • Fluent English
  • Valid driver’s license
  • Ability to travel internationally and domestically

Work Rights

Not specified

Tailored Resume

Cover Letter