As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level
Job Summary
As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level.
You will work closely with clinical teams, providing guidance and support to ensure that sites meet regulatory and operational requirements while delivering high-quality data and achieving study goals.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
Matching Summary
As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level.
Skills & Requirements
Must-have
Overseeing site management activities
Ensure compliance with protocols and regulations
Collaborate with clinical teams
Resolve site-level issues
Prepare site management documentation
Nice-to-have
Foster collaboration and process improvement
Nurture talent and reward high performance
Inclusive and accessible environment
Key Requirements
Bachelor's degree in life sciences, clinical research, or related field
Extensive experience in site management, clinical operations, or monitoring
Strong understanding of clinical trial processes, GCP, and regulatory requirements
Excellent problem-solving and organizational skills