Guide daily oversight of international clinical trials to deliver on time and budget.
Develop and execute plans for in-house oncology trial management.
Collaborate with data management, regulatory and investigators for high-quality data.
Manage trial start-up: site selection, feasibility, and documentation prep.
Ensure site initiation, training, and monitoring per ICH-GCP guidelines.
Monitor progress, identify risks, and implement corrective actions.

🎯 Requirements

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

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