Senior Clinical Research Associate
ICON
ICON seeks a Senior Clinical Research Associate to monitor clinical trial progress at investigative sites or remotely, ensuring studies are conducted and reported per protocol, SOPs, ICH-GCP standards, and regulatory requirements. This home-based role is based in Montreal or Burlington, Canada.
Responsibilities
- Monitor progress of clinical studies at investigative sites or remotely
- Ensure clinical trials are conducted in accordance with protocol and ICH-GCP standards
- Verify clinical trial data is recorded and reported per SOPs and regulatory requirements
- Maintain compliance with applicable regulatory requirements throughout trial execution
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
- Knowledge of ICH and local regulatory authority regulations for drug trials
- Oncology monitoring experience preferred
- Ability to travel 70%
- Bilingual English/French required
- Legal authorization to work in United States or Canada; no visa sponsorship needed
Vacancy posted 2 days ago
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