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The Manager of Regulatory Affairs develops and leads regulatory strategies for medical devices, ensuring compliance with global regulatory authorities. This role involves submissions for FDA approvals, managing cross-functional teams, and aligning regulatory strategies with business objectives while maintaining communication with executive leadership.

The Project Director will lead cross-functional teams in oncology clinical research, managing project timelines, budgets, and regulatory compliance. Responsibilities include client collaboration, overseeing project deliverables, and ensuring proper training and resource allocation throughout the project lifecycle.

The Senior Project Director is responsible for leading cross-functional project teams in oncology clinical research studies. This role involves managing project scope, timelines, budgets, and regulatory compliance while providing mentorship and acting as the primary contact for clients. Additionally, they facilitate effective teamwork and ensure the delivery of project objectives within specified guidelines.