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Manage regional study delivery, oversee clinical operations, ensure compliance and inspection readiness, and collaborate with stakeholders to meet study goals.

The Director will manage global regulatory strategies and processes, provide leadership on regulatory issues, and interface with business partners and regulatory authorities to secure product approvals and market access.

Lead and mentor oncology program management teams, develop global product strategies, manage projects, and drive process improvements in drug development.

Manage biomarker operational work for clinical trials, oversee junior project managers, and collaborate with internal and external stakeholders to ensure project success.

The role involves leading global forecasting and performance management, setting standards, overseeing processes, collaborating with cross-functional teams, and developing a high-performing team in the oncology biotech sector.