Serve as the primary point of contact between investigational sites and the sponsor for Oncology trials, conducting all types of site visits and ensuring compliance with regulations
Job Summary
Serve as the primary point of contact between investigational sites and the sponsor for Oncology trials, conducting all types of site visits and ensuring compliance with regulations.
Monitor patient safety, oversee drug accountability, resolve data queries, and support subject recruitment and retention efforts at the site level.
ICON offers a competitive salary, diverse benefits including health insurance, retirement planning, and employee assistance programs, fostering a culture of inclusion and rewarding high performance.
Matching Summary
Serve as the primary point of contact between investigational sites and the sponsor for Oncology trials, conducting all types of site visits and ensuring compliance with regulations.
Skills & Requirements
Must-have
Oncology clinical trials monitoring
ICH-GCP and regulatory compliance
CTMS and eTMF systems proficiency
Site selection and initiation visits
Routine monitoring and close-out visits
Patient safety and AE/SAE reporting
Nice-to-have
Collaborative team player
Clear communicator and problem-solver
Fostering an inclusive environment
Driving innovation and excellence
Key Requirements
2+ years on-site monitoring experience
Bachelor's degree in Life Sciences or RN
Eligible to work in United States
Travel up to 50% for monitoring visits
Work Rights
Eligible to work in United States without visa sponsorship