ICON plc is a world-leading healthcare intelligence and clinical research organisation advancing clinical research from molecule to medicine
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organisation advancing clinical research from molecule to medicine.
As a Clinical Research Associate, you will monitor clinical studies at investigative sites or remotely ensuring compliance with protocols and regulatory standards.
ICON offers a comprehensive and competitive total reward package including base pay, variable pay, recognition programs, and best-in-class employee benefits tailored to support employees and their families.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organisation advancing clinical research from molecule to medicine.
Skills & Requirements
Must-have
Clinical study monitoring
Knowledge of ICH-GCP guidelines
Ability to travel 70%
Oncology monitoring experience
Remote and onsite site monitoring
Nice-to-have
Bilingual English/French
Inclusive and supportive work culture
Continuous learning environment
Patient-centered clinical research
Key Requirements
Bachelor's degree or equivalent in scientific or health-related field
1+ years clinical monitoring experience for level 2 role; 3+ years for level 3
Legal authorization to work in US or Canada without visa sponsorship
Bilingual English/French required
Oncology monitoring experience preferred
Work Rights
Legally authorized to work in US or Canada without sponsorship