Teams 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 QA Manager, Document Control will oversee Document Control and quality system maintenance, system administration of MasterControl EQMS, training, and managing controlled documents.

The Clinical Data Manager oversees data management activities across clinical studies, ensuring data compliance and quality from start-up to closure, while managing CRO vendors and leading the data management team.