Clinical Trial Manager Consultant - II

📋 Description

• Guide and oversee international clinical trials, delivering quality data on time and on budget.
• Develop and execute operational plans for oncology trial management.
• Collaborate with cross-functional teams to ensure operational excellence and timely data.
• Manage trial startup activities with Site Engagement & Monitoring Excellence and SRM to deliver site selection and feasibility.
• Collaborate on site initiation, training, and monitoring per protocol and ICH-GCP.
• Monitor progress, identify risks and deviations, and implement corrective actions to maintain timelines and study integrity.

🎯 Requirements

• Bachelor's or advanced degree in a relevant scientific discipline.
• At least 3 years in Clinical Operations; oncology trial management preferred.
• Knowledge of ICH-GCP and FDA requirements, oncology research.
• Experience managing trials from start-up to closeout.
• Strong project management skills; ability to prioritize tasks, allocate resources, and manage timelines and budgets.
• Proficiency with Veeva CTMS preferred.