Senior CRA
ICON
ICON seeks a Senior Clinical Research Associate for its Montreal office to oversee clinical trial progress at investigative sites or remotely. The role ensures studies are conducted and reported in compliance with protocol, ICH-GCP guidelines, and regulatory standards.
Responsibilities
- Monitor progress of clinical studies at investigative sites or remotely
- Ensure clinical trials conducted, recorded, and reported per protocol and SOPs
- Verify compliance with ICH-GCP and applicable regulatory requirements
- Maintain documentation standards throughout trial conduct and reporting
Requirements
- Bachelor's degree in scientific or health-related field, or equivalent education and clinical research experience
- 1+ years clinical monitoring experience for level 2 role; 3+ years for level 3 role
- Fluent in both French and English
- Knowledge of ICH guidelines and local regulatory authority drug trial regulations
- Ability to travel 70%
- Legal authorization to work in United States or Canada; no visa sponsorship required
- Oncology monitoring experience preferred
Vacancy posted a month ago
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