ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation, excellence, and inclusivity
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation, excellence, and inclusivity.
The role involves monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards while supporting successful trial execution.
ICON offers competitive salary and benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation, excellence, and inclusivity.
Skills & Requirements
Must-have
Oncology clinical trial monitoring
Good Clinical Practice (GCP) standards
Clinical trial site management
Data collection and reporting
Travel up to 60% internationally and domestically
Valid driver’s license
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder relationship management
Strong organizational and problem-solving skills
Excellent communication and interpersonal skills
Inclusive and diverse work culture
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Five years of CRA experience with oncology monitoring