ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
As a Senior Clinical Research Associate at ICON, you will play a critical role in overseeing clinical trial sites to ensure compliance with protocols, regulatory requirements, and GCP standards while ensuring participant safety and data integrity.
ICON offers competitive salary and a range of 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 fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Clinical trial site monitoring
Good Clinical Practice (GCP) standards
On-site monitoring and source data verification
CTMS platform proficiency
Phase I oncology trial expertise
International and domestic travel up to 60%
Trip report writing
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder relationship management
Experience with PARP inhibitors
Inclusive and diverse work culture
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive CRA experience with clinical trial processes
Valid driver’s license
Experience with breast, ovarian, prostate, and pancreatic cancer trials