As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight
Job Summary
As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight.
This role will have no interaction with sites and will not conduct site visits.
ICON is committed to providing a workplace free of discrimination and harassment.
Matching Summary
As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight.
Skills & Requirements
Must-have
Experience in clinical monitoring
Strong focus on data quality
Regulatory compliance expertise
Nice-to-have
Excellent communication skills
Ability to manage multiple projects
Collaborative team player
Key Requirements
Advanced degree in life sciences
At least 1 year experience reviewing Monitoring Visit Reports