Shape the future of HIV treatment by building strong relationships with healthcare providers, driving sales growth, and delivering essential clinical information to maximize patient outcomes in the assigned territory.

Lead transformational efforts in regulatory submissions by overseeing cross-functional integration, project management, and strategy alignment. Drive organizational readiness and operational excellence to achieve critical filing milestones effectively.

Lead a high-performing team in the execution of major regulatory submissions while ensuring cross-functional alignment and operational excellence, driving timely and quality outcomes in a fast-paced pharmaceutical environment.

Elevate quality compliance across global operations by leading audit teams, ensuring adherence to regulations, and fostering a culture of continuous improvement to enhance manufacturing processes and systemic quality oversight.

Support late-stage oncology clinical development by collaborating on trial activities, preparing protocols, and contributing to regulatory submissions, while adhering to Good Clinical Practice and industry standards throughout the process.