Teams at Obsidian Therapeutics

Lead Quality Control activities for a clinical-stage autologous cell therapy program, ensuring compliance and operational readiness while establishing QC strategies and overseeing external partners.

The role involves managing document control and training processes to ensure compliance with regulations. Responsibilities include overseeing GxP document lifecycle and training programs, supporting audits, and collaborating with stakeholders to implement systems and processes.

Lead data management for clinical studies, ensuring compliance with regulatory standards, database setup, and effective collaboration across teams to deliver data on time.