Jobs at Adverum Biotechnologies

Support design and execution of clinical development activities for ophthalmology trials: protocol writing, vendor/CRO oversight, medical monitoring, data review/interpretation, regulatory document contributions, and cross-functional collaboration.

The QC Analyst will perform quality control reviews of various assays, ensuring compliance with GxP requirements and supporting investigations and validations in a regulated lab environment.

The Principal Scientist will optimize AAV downstream processes, lead purification development, support regulatory compliance, and collaborate across functions for gene therapy programs.