As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Job Summary
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
ICON offers a diverse and inclusive culture that rewards high performance and nurtures talent, providing competitive salary and a range of benefits focused on well-being and work-life balance.
ICON is committed to providing an inclusive and accessible environment for all candidates and ensures equal employment consideration without discrimination.
Matching Summary
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Skills & Requirements
Must-have
Clinical trial site monitoring
Good Clinical Practice (GCP) compliance
Oncology clinical studies experience
Early phase clinical trial experience
Home-based work arrangement
International and domestic travel up to 60%
Site management and data integrity
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Strong organizational and problem-solving skills
Excellent communication and interpersonal skills
Stakeholder relationship management
Proficiency in clinical trial software
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Minimum 5 years SIT onsite monitoring experience
Valid driver’s license
Experience managing multiple sites and projects
Global oncology studies experience
Ability to travel at least 60% internationally and domestically