You will work closely with the team, internal colleagues (scientific, legal, and financial), and external collaborators (CROs, and sometimes academics or biotech and pharmaceutical companies) on all aspects of CHDI’s clinical research and development efforts, with a particular focus on the operational planning, coordination, and delivery of complex, multi-vendor studies. A Clinical Research Program Manager works closely with study teams, Directors, and others within CHDI in the following areas: Vendor management Lead end‑to‑end vendor management: selection, onboarding, contract negotiation, renewals, and termination.