Provide guidance and daily oversight for international clinical trials; on time and on budget.
Develop and execute operational plans for oncology trial management.
Collaborate with cross-functional teams to ensure rapid, high-quality data.
Manage trial start-up activities: site selection, feasibility, and documentation.
Collaborate with Site Engagement & Monitoring Excellence on initiation, training, and monitoring.
Monitor study progress; identify risks and implement corrective actions.

🎯 Requirements

Bachelor's or advanced degree in a relevant scientific discipline.
5+ years in Clinical Operations; oncology trial mgmt experience preferred.
Deep knowledge of ICH-GCP and FDA requirements for oncology.
Proven track record in managing trials from start-up to closeout.
Strong project management: prioritization, resource allocation, budgets.
Proficiency with Veeva CTMS; CTMS experience preferred.

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