Teams at BlueRock Therapeutics

Lead process development to adapt PSC-derived neurology cell processes from research scale to GMP/GLP standards. Optimize scale-up platforms, perform raw materials risk assessments, generate GLP-grade cell supplies for pre-IND studies, prepare/review experimental proposals and SOPs, mentor junior staff, analyze experimental data to support decisions, and present results to colleagues.

Lead clinical data management for studies including CRO oversight, eCRF/EDC development, data cleaning and reconciliation, database lock and archiving, metrics tracking, UAT, and mentoring data managers to ensure timely, inspection-ready data deliverables.

Lead bench-level development and optimization of characterization and quality assays for cell therapy products. Design and run in vitro experiments, perform flow cytometry, ELISA, PCR and other assays, analyze and trend data, establish specifications, review SOPs/protocols, ensure regulatory compliance, and support technology transfer and presentations.