Clinical Research Associate II at ICON plays a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments
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 innovative treatments.
The role involves conducting site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and patient safety.
ICON offers a diverse culture with competitive salary and benefits focused on well-being, work-life balance, and inclusion.
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 innovative treatments.
Skills & Requirements
Must-have
Clinical trial site visits
Protocol compliance monitoring
Data review and query resolution
Travel at least 60% of the time
ICH-GCP guidelines knowledge
Nice-to-have
Strong organizational skills
Effective communication skills
Ability to work independently and collaboratively
Attention to detail
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years Clinical Research Associate experience
Valid driver’s license
Ability to travel internationally and domestically