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The LEAP Associate role aims to accelerate the development of commercial leaders through structured rotations in sales, marketing, and market access, with a focus on strategic execution and AI integration in commercial initiatives.

The Operations Supervisor oversees daily production in a CAR-T cell therapy environment, ensuring compliance with cGMP regulations and leading a team to meet operational goals.

Lead organization design, change management, and leadership development initiatives to improve organizational effectiveness. Partner with business leaders and HRBPs on workforce planning, talent and promotion processes, performance systems, and measurement of OD impact. Drive global programs, culture, and capability building for sustainable growth.

The Senior Clinical Trial Associate will support the execution of Phase I/II CAR-T oncology trials, ensuring compliance with regulations and coordinating trial activities.

The Preclinical Scientist will conduct preclinical pharmacology and toxicology studies to support cell therapy development, design assays, and prepare scientific documents in a collaborative environment.

The Sr. QC Analyst is responsible for completing QC testing for cell therapy products, ensuring compliance with procedures and GMP regulations, conducting analytical testing, and collaborating within the Quality team.

The Associate Director will oversee performance reporting and dashboard development, ensuring data-driven insights for commercial decision-making and automating reporting processes using advanced analytics and AI.

The Sr. Manager, Commercial Training will develop and implement training for new hires and ongoing needs, conduct field rides, analyze feedback, and assess training gaps within regions. This role requires collaboration with sales management and continuous professional development of commercial field teams with a focus on instructional efficacy and compliance.

The Principal Scientist will lead clinical biomarker projects in immunology and immuno-oncology for hematological malignancies, designing clinical studies and overseeing data analysis.

The QC Specialist is responsible for sample management, documentation, and ensuring compliance with cGMP in the QC laboratory. They prepare documents, manage samples, and support audits while working independently and collaboratively as a technical specialist.