FSP Clinical Research Associate I - Bilingual French QC Canada

Thermo Fisher Scientific seeks a Clinical Research Associate I to conduct remote and on-site monitoring of investigational sites across clinical trials. The role involves assessing protocol compliance, managing documentation, and collaborating with trial sites to ensure data accuracy and regulatory adherence. Bilingual French and English fluency required.

Responsibilities

• Monitor investigator sites using risk-based approach; identify process failures and implement corrective actions
• Conduct source data review, verification, and CRF review through on-site and remote monitoring activities
• Assess investigational product inventory and records; document observations in reports and escalate deficiencies
• Conduct site initiation and close-out activities; ensure essential documents complete and compliant
• Facilitate communication between sites, sponsor companies, and internal teams; maintain trial status tracking

Requirements

• Bachelor's degree in life sciences or RN certification with equivalent qualification
• Approximately 2 years clinical monitoring or clinical trial experience
• ICH-GCP and applicable regulatory knowledge and compliance familiarity
• Fluent English and French written and oral communication
• Strong critical thinking and root cause analysis capabilities
• Proficiency with Microsoft Office and ability to learn trial management software
• Valid driver's license where applicable