FSP Sr. CRA - Oncology Experience - US West

Senior Clinical Research Associate position supporting oncology trials across investigational sites in a remote capacity. Responsibilities include risk-based monitoring, protocol compliance assessment, data quality review, and site management to ensure regulatory adherence and subject safety.

Responsibilities

• Conduct remote and on-site monitoring visits to assess protocol compliance and regulatory adherence
• Review source documents, data records, and case report forms for accuracy and completeness
• Perform investigational product inventory assessments and records verification
• Identify process failures and implement corrective/preventive actions with sites
• Prepare monitoring reports, trip reports, and trial status updates for clinical management

Requirements

• Bachelor's degree in life sciences or RN certification with relevant qualification
• 2+ years clinical research monitoring experience or equivalent
• Strong understanding of ICH-GCP guidelines and applicable regulations
• Critical thinking and root cause analysis skills for problem-solving
• Excellent written and oral communication abilities
• Risk-based monitoring knowledge and experience
• Valid driver's license where applicable