Clinical Monitoring Operations Manager

📋 Description

• Oversee monitoring strategy from study start-up to close-out.
• Lead alliance management and optimize monitoring operations.
• Primary contact for interim analyses, DB locks, milestones.
• Manage documents: Monitoring Plan, eCRFs, SOPs.
• Ensure monitoring deliverables stay on time, within scope and budget.
• Track KPIs, dashboards, and risk with stakeholder reporting.

🎯 Requirements

• Bachelor's degree in business, life sciences, or related field.
• 5–7 years in clinical research, PM, and monitoring ops; PMP preferred.
• 4+ years managing clinical projects across full trial lifecycle.
• Deep knowledge of ICH-GCP, FDA, and global regulatory standards.
• Proficiency with EDC, TMF, CTMS, and IRT systems; KPI reporting.
• Strong communication, leadership, and cross-functional collaboration.

🎁 Benefits

• Global CRO with career development and client-facing roles.
• Equal opportunity employer; diverse and inclusive culture.