Serve as the primary point of contact between investigational sites and the sponsor for Oncology TA
Job Summary
Serve as the primary point of contact between investigational sites and the sponsor for Oncology TA.
Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out, ensuring site compliance with ICH-GCP, SOPs, and regulations.
ICON offers a range of benefits designed to be competitive, focused on well-being and work-life balance, including various annual leave, health insurance, retirement planning, and a Global Employee Assistance Programme.
Matching Summary
Serve as the primary point of contact between investigational sites and the sponsor for Oncology TA.
Skills & Requirements
Must-have
On-site monitoring experience
ICH-GCP and regulations
CTMS and eTMF systems
Patient safety monitoring
Drug accountability oversight
Site compliance maintenance
Nice-to-have
Clear communicator
Problem-solver
Collaborative team player
Inclusive environment fostering innovation
Key Requirements
2+ years on-site monitoring experience
Bachelor's degree in Life Sciences or equivalent, or RN
Eligible to work in United States without visa sponsorship
Experienced monitoring oncology trials
Work Rights
Eligible to work in United States without visa sponsorship