In this important leadership role, the head of program management will be responsible for developing the program management function, including approaches that will align functions, program teams, and leadership toward delivery of integrated corporate and program goals. A near term priority will be to assist senior management in long-term planning processes including understanding of forward-looking cross program and portfolio projections. At the outset, the head of program management will support therapeutic program leadership to build program delivery capabilities. Though the vision is to build a PM team as soon as possible, a hands-on role at the project team level will be necessary in the near term. Over time, the head of PM will evolve and scale the program management function to keep pace with AlloVir’s organizational growth. The ideal candidate will have a hands-on approach, strong leadership skill, and shares our team’s determined, positive attitude.

The Director of Regulatory Affairs will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for product development and approval, in alignment with the global business strategy. Responsible for leading a comprehensive and strategic approach to developing and executing integrated global regulatory strategies that account for the complex interplay between major Health Authorities. Represent the company with domestic and international regulatory authorities, contractors and corporate partners. Provide regulatory support for various departments, projects, and teams/committees.

In this important Clinical Development Operations role, clinical project management is responsible for collaborating with clinical and regulatory functions to execute on clinical strategies to deliver successful operational outcomes across one or multiple clinical trials. In addition to exceptional project delivery, we seek strong analytical skill, attention to detail, and leadership qualities that will influence our internal team and motivate our CRO partners. The ideal candidate values bringing important medicines to patients in need, and shares our team’s determined, positive attitude

In this important Clinical Development Operations role, the Clinical Project Associate/ Clinical Project Specialist is responsible for collaborating with the AlloVir and contract research organization (CRO) clinical project teams across multiple clinical trials. The main role of the CPA/ CPS is to ensure TMF compliance and trial organization by careful review of essential documents, organizing meetings and tracking action items, as well as setting up document review workflows and SharePoint file structures. This role will oversee large amounts of documents and information; as such requires a very high attention to detail, the ability to organize process flows and workstreams, and strong analytical skill. The ideal candidate values bringing important medicines to patients in need, and shares our team’s determined, positive attitude.