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.
ICON offers a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
ICON is committed to providing an inclusive and accessible environment for all candidates and ensuring a workplace free of discrimination and harassment.
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
Clinical trial site monitoring
Protocol compliance and data integrity
Patient safety management
Collaboration with investigators and site staff
Data review and query resolution
Travel at least 60% internationally and domestically
Valid driver’s license
Nice-to-have
Strong organizational skills
Excellent communication skills
Ability to work independently and collaboratively
Attention to detail
Fast-paced environment adaptability
Inclusive and diverse culture
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years Clinical Research Associate experience
In-depth knowledge of clinical trial processes and ICH-GCP guidelines