Clinical Research Associate

ICON plc

Singapore, Singapore
Monitoring clinical trials
Compliance with regulations
Data collection and analysis
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • You will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.
  • ICON offers a range of additional benefits focused on well-being and work-life balance opportunities for you and your family.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • monitoring clinical trials
  • compliance with regulations
  • data collection and analysis

Nice-to-have

  • strong stakeholder relationships
  • excellent communication skills
  • collaborative team environment

Key Requirements

  • At least 2 years of monitoring experience
  • University degree in medicine or science
  • Knowledge of ICH-GCP guidelines
  • Ability to travel at least 60% of the time

Work Rights

Not specified

Tailored Resume

Cover Letter