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The role entails managing global labeling strategies, ensuring compliance with regulations, leading cross-functional teams, and preparing regulatory documents for pharmaceuticals.

Manage vendor contracts for clinical trials, conduct negotiations, ensure cost-effective agreements, oversee contract execution, and improve procurement processes.

The Director leads oncology pricing and contracting strategies, ensuring market access and alignment across internal teams while monitoring product pricing and implementing strategic initiatives.

Provide strategic legal support for U.S. oncology products, negotiate contracts, manage outside counsel, and mentor junior legal staff.

Provide strategic legal support for market access, including contract negotiation, compliance with pricing regulations, and mentorship within the Legal Affairs Department.

Responsible for developing relationships with stakeholders, leading strategic sourcing, supplier negotiations, and enhancing procurement capabilities within global operations.

The CMC Lead manages project teams and strategies within pharmaceutical drug development, focusing on budget, timeline, and stakeholder communication.