Job Description

Fortrea seeks Clinical Trial Managers with 3+ years of experience to oversee clinical research trial delivery and operations. The role manages study start-up, site activation, regulatory submissions, and financial aspects while ensuring compliance with GCP and regulatory standards. Remote position based in the US or Canada.

Responsibilities

• Manage end-to-end study oversight from site identification through database lock, including timelines and budget
• Lead site activation, identification, and recruitment strategies; oversee CTA development and negotiation
• Manage regulatory and ethics committee submissions, approvals, and tracking throughout study duration
• Ensure financial controls, revenue forecasting, and scope adherence; oversee site payments and reconciliation
• Implement risk management strategies, monitor KPIs, and maintain inspection readiness of trial documentation

Requirements

• Bachelor's degree in life science or allied health certification (nursing, medical, laboratory technology)
• Four or more years of clinical research experience in pharmaceutical, CRO, or healthcare setting
• Previous SSU and Clinical Trial Lead experience
• Comprehensive knowledge of GCP, ICH, and regulatory guidelines
• Proficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF platforms
• Strong leadership, communication, and organizational abilities in remote and global environments
• Fluent in English, both written and verbal

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