Clinical Research Associate

ICON

Bangkok, Thailand
Onsite
Site qualification, initiation, monitoring, and close-out
Protocol compliance and data integrity
Patient safety throughout the trial
As a Clinical Research Associate II at ICON, you will play 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

  • As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, 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 Clinical Research Associate II at ICON, you will play 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

  • Site qualification, initiation, monitoring, and close-out
  • Protocol compliance and data integrity
  • Patient safety throughout the trial
  • Collaborating with investigators and site staff
  • Data review and query resolution

Nice-to-have

  • Inclusive environment driving innovation
  • Diverse and dynamic team
  • Advancement of innovative treatments

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years onsite monitoring CRA experience
  • Knowledge of clinical trial processes, regulations, ICH-GCP

Work Rights

Not specified

Tailored Resume

Cover Letter