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The Senior Associate Scientist will develop and optimize CAR-T manufacturing processes, conduct experiments, and support technology transfers for clinical applications.

The role involves developing and characterizing manufacturing processes for CAR T therapies, conducting experiments, documenting results, and supporting GMP initiatives.

The Executive Director, Market Access will develop and lead market access strategy for CAR T therapies, focusing on pricing, reimbursement, and payer engagement. Responsibilities include establishing payer relationships, negotiating coverage terms, and implementing patient support services to enhance access and value for patients and providers.

The Senior Scientist will develop and characterize CAR-T products, supporting analytical methods, ensuring quality in GMP manufacturing, and collaborating with stakeholders.

Lead product characterization strategy for CAR T cell therapy, collaborating with various stakeholders and ensuring compliance with regulatory guidelines.

The Senior Associate Scientist will develop and characterize clinical-scale CAR T therapies, support analytical methods, ensure adherence to regulatory standards, and collaborate with internal stakeholders.

The Senior Counsel will manage corporate legal functions including SEC reporting, corporate governance, and strategic transactions, while advising executives and overseeing compliance matters.

The Associate Director of Data Science will lead quality data science initiatives, develop strategies for product quality control, provide analytical insights, and support regulatory compliance in a biotechnology setting.

Lead the Process Sciences group, driving innovation in cell therapy technologies and managing teams for Drug Substance and Drug Product processes. Engage in project management and regulatory strategy development, with a focus on high-quality production and mentoring staff.

The Director of Translational Operations will oversee biospecimen operations in clinical programs, manage internal teams and vendors, ensure compliance, and develop operational strategies for clinical trials.