Serve as the primary point of contact between investigational sites and the sponsor, conducting all types of site visits
Job Summary
Serve as the primary point of contact between investigational sites and the sponsor, conducting all types of site visits.
Ensure site compliance with ICH-GCP, SOPs, and regulations, while monitoring patient safety and resolving data queries.
ICON offers a range of benefits designed to be competitive and focused on well-being and work-life balance, including various annual leave entitlements and health insurance offerings.
Matching Summary
Serve as the primary point of contact between investigational sites and the sponsor, conducting all types of site visits.
Skills & Requirements
Must-have
On-site monitoring experience
Hematology oncology clinical trials
ICH-GCP compliance
CTMS and eTMF systems
Patient safety monitoring
Drug accountability oversight
Nice-to-have
Clear communicator
Problem-solver
Collaborative team player
Inclusive environment
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
Travel up to 50% for monitoring visits
Work Rights
Eligible to work in United States without visa sponsorship