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.
You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
Monitoring clinical trial sites, conducting site visits, collaborating with cross-functional teams, and providing training and guidance are key responsibilities of this role.
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) standards
Phase I oncology monitoring experience
Travel at least 60% of the time
Data integrity and site management
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
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Five years of CRA experience
Phase I oncology monitoring experience
Must be located in LA or SF Bay area; San Diego, Oregon, Utah considered