Senior Clinical Research Associate
usd108.58k - usd135.72k per yearICON
ICON seeks a Senior Clinical Research Associate to monitor clinical trials at investigative sites or remotely, ensuring compliance with protocols, SOPs, ICH-GCP guidelines, and regulatory requirements. The role supports the acceleration of drug and device development across multiple Canadian locations.
Responsibilities
- Monitor progress of clinical studies at investigative sites or remotely
- Ensure clinical trials are conducted and documented according to protocol and SOPs
- Verify compliance with ICH-GCP and applicable regulatory requirements
- Report trial progress and findings in accordance with regulatory standards
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; 3+ years for Level 3
- Knowledge of ICH and local regulatory authority regulations for drug trials
- Legal authorization to work in United States or Canada; no visa sponsorship required
- Ability to travel 70%
- Oncology monitoring experience preferred
- Bilingual English/French required (per Canadian posting)
Vacancy posted 7 hours ago
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