As a CRA II/Senior CRA 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 CRA II/Senior CRA 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 global employee assistance programs.
ICON is committed to providing an inclusive and accessible environment free of discrimination and harassment, encouraging all qualified applicants to apply regardless of background or experience.
Matching Summary
As a CRA II/Senior CRA 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
collaborating with investigators
data review and query resolution
ability to travel at least 60%
Nice-to-have
strong organizational skills
effective communication skills
ability to work independently and collaboratively
attention to detail
inclusive and diverse work culture
Key Requirements
Bachelor’s degree in scientific or health-related field
Minimum 1 year independent monitoring for CRA II
Minimum 3 years independent monitoring for Senior CRA
In-depth knowledge of clinical trial processes and ICH-GCP guidelines
Valid driver’s license
Ability to travel internationally and domestically