Clinical Research Associate

ICON Clinical Research, LP

Singapore, Singapore
Overseeing and coordinating clinical trials
Ensuring compliance with regulations
Collecting and analyzing critical data
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.
  • As a key member of our research department, 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 designed to be competitive within each country and focused on well-being and work life balance opportunities.

Matching Summary

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

Skills & Requirements

Must-have

  • overseeing and coordinating clinical trials
  • ensuring compliance with regulations
  • collecting and analyzing critical data
  • maintaining study documentation
  • patient safety compliance

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • strong collaborative relationships
  • deal with queries in a timely manner

Key Requirements

  • At least 2 years of monitoring experience as a CRA
  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines
  • Ability to travel at least 60% of the time
  • Possess a valid drivers license

Work Rights

Not specified

Tailored Resume

Cover Letter