Director/Associate Director, R&D Quality, PV
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About The Position
At Viridian Therapeutics, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets. Reporting to the Senior Director, R&D Quality the Director/Associate Director, R&D Quality PV will collaborate closely with cross-functional teams, including PV, Regulatory Affairs, Clinical, and Legal. The Quality Assurance AD/Director overseeing Pharmacovigilance (PV) and Safety, as well as clinical trial oversight is a critical leadership role responsible for ensuring operational quality and compliance with global regulatory requirements, industry standards, and company policies. This role involves designing, implementing, and managing quality systems and processes to support drug safety, pharmacovigilance and clinical trial oversight activities, ensuring subject safety, and maintaining the highest quality standards across the organization. This role may be based in Waltham, MA, which would be a hybrid role, or it can also be fully remote. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
