Tim joined ARM as CEO in 2022 with more than 20 years of experience in the biotechnology industry. A company-builder with a focus on corporate culture, he has helped early-stage organizations create internal cohesion and advance strategic initiatives. As chief executive, Tim divides his time between managing ARM and its global staff of nearly 30 employees and serving as an external advocate on behalf of ARM’s membership and the broader cell and gene therapy sector. Tim was most recently the Chief Culture and Corporate Affairs Officer at Xilio Therapeutics, a biotechnology company developing tumor-selective immuno-oncology therapies for patients with cancer. Prior to that, he was the Chief Corporate Affairs Officer at CRISPR gene-editing pioneer Editas Medicine, where he led the company’s global policy and government affairs, bioethics, communications, market development and human resources initiatives. He also served in executive public affairs roles at Cubist Pharmaceuticals and Biogen. Tim was an Advisory Group member of the Value-Based Payments for Medical Products consortium at the Duke-Margolis Center for Health Policy. He also has been a member of the Board of Directors of the non-profit organization Life Science Cares and has chaired the Ethics Committee of the American Society of Gene and Cell Therapy (ASGCT). Tim is also no stranger to the ARM network. He previously served as a member of ARM’s Gene Editing Task Force and on the Biotechnology Innovation Organization’s Gene Editing Working Group. Tim received a B.A. in history and philosophy from Boston College and a J.D. from the Columbus School of Law at the Catholic University of America. He lives in Boston with his wife and children and is a passionate fan of the Boston Celtics.
In this illuminating keynote panel, we will explore real experiences of navigating the regulatory and reimbursement framework at an EU and global level to bring innovative therapies to people with rare conditions. Leading stakeholders will share their insights on creating sustainable and effective models that ensure equitable access to life-saving therapies. Join us for this engaging session as we seek to redefine the future of orphan drug development and delivery, focusing on sustainability, equity, and innovation in the quest for better outcomes for patients with rare diseases.