Clinical Research Associate - Remote - Sponsor Dedicated
ICON
Greece
Clinical trial monitoring
Protocol compliance
Data integrity management
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 options, retirement planning, and a global employee assistance program.
ICON is dedicated to providing an inclusive and accessible environment, committed to a workplace free of discrimination and harassment, and encourages all qualified applicants to apply regardless of whether they meet all requirements.
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 monitoring
protocol compliance
data integrity management
patient safety oversight
site qualification and initiation
travel up to 60%
valid driver’s license
Nice-to-have
strong organizational skills
effective communication
collaborative work style
attention to detail
inclusive work environment
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years Clinical Research Associate experience
In-depth knowledge of ICH-GCP guidelines
Ability to travel internationally and domestically