ICON is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development
Job Summary
ICON is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Responsibilities include supporting site activation by managing regulatory documents, coordinating translations, and ensuring timely data entry into tracking systems.
ICON offers competitive benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.
Matching Summary
ICON is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Skills & Requirements
Must-have
ICON SOPs/WPs
ICH/GCP
regulatory processes
document review
site activation tasks
TMF quality control
Nice-to-have
culture of quality
process improvement
work life balance
inclusive environment
team collaboration
Key Requirements
Bachelor’s Degree in Life Sciences
Minimum 2 years clinical study start up experience
Knowledge of local/international regulatory processes
Ability to read clinical protocols
Excellent English and Spanish communication skills