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 diverse and inclusive culture that rewards high performance and nurtures talent, providing competitive salary and a range of benefits focused on well-being and work-life balance.
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 site monitoring
Protocol compliance assurance
Data review and query resolution
Travel availability at least 60%
Collaboration with investigators
Nice-to-have
Strong organizational skills
Effective communication skills
Ability to work independently
Fast-paced environment adaptability
Attention to detail
Key Requirements
Bachelor's degree in scientific or healthcare-related field
Minimum 2 years experience as Clinical Research Associate
In-depth knowledge of clinical trial regulations and ICH-GCP