🛠 Tech Stack

💼 About This Role

You'll oversee site monitoring and management across early-phase oncology studies, ensuring regulatory compliance and data integrity. This fully remote role offers field flexibility while contributing to cutting-edge clinical trials that advance patient outcomes.

🎯 What You'll Do

• Manage and monitor oncology clinical trial sites for compliance with protocols and GCP.
• Conduct remote and on-site monitoring visits (qualification, initiation, interim, close-out).
• Serve as primary liaison between clinical teams and investigative sites.
• Ensure inspection readiness with accurate documentation and TMF reconciliation.

📋 Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• 5+ years of independent oncology clinical trial monitoring experience.
• 1+ year supporting early development clinical studies.
• Knowledge of oncology research processes, GxP guidelines, and risk-based monitoring.

✨ Nice to Have

• Familiarity with Veeva systems.
• Experience with functional service provider models.
• Bilingual proficiency in French and English.

🎁 Benefits & Perks

• 🏖️ Fully remote work with field flexibility.
• 💰 Competitive salary package.
• 🏥 Comprehensive health insurance for employees and families.
• 📈 Retirement savings and long-term financial planning programs.
• 🌍 Global Employee Assistance Program with 24/7 well-being resources.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical/Behavioral Interview· 60 min