Transform the landscape of clinical quality assurance by leading initiatives that ensure compliance with GCP and regulatory standards. Collaborate with cross-functional teams to fortify a culture of quality in innovative cell therapy development.

Champion quality control excellence, overseeing testing and compliance for cellular drug products. Lead a high-performing QC team to ensure readiness and adherence to cGMP in a dynamic, collaborative environment dedicated to innovation.

Elevate clinical data management efforts across oncology programs by leading data review activities, collaborating with cross-functional teams, and ensuring high-quality datasets are generated for safety assessments and regulatory submissions.

Strategize and lead biostatistics for clinical development from Phase 1 to commercialization. Collaborate cross-functionally, ensuring scientific integrity and regulatory compliance while shaping the future of advanced therapies in oncology.

Drive excellence in clinical supply chain operations, ensuring efficient and compliant management of drug products for clinical trials while fostering collaboration across teams and external partners to meet project timelines.