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 additional 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 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 monitoring and site visits
Protocol compliance and patient safety
Data review and query resolution
Ability to travel at least 60%
Valid driver’s license required
Nice-to-have
Strong organizational and communication skills
Ability to work independently and collaboratively
Inclusive and diverse work environment
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years Clinical Research Associate experience
In-depth knowledge of clinical trial regulations and ICH-GCP
Valid driver’s license
Ability to travel internationally and domestically