Director Clinical Development

Role: Lead clinical development strategy and medical oversight for oncology programs, focusing on immuno-oncology. Responsibilities include designing innovative trial protocols, shaping development plans, managing CRO relationships, providing medical monitoring, and contributing to regulatory submissions and publications. The role involves building external relationships with key opinion leaders, supporting collaboration efforts, and participating in regulatory interactions. It also includes strategic input on biomarker and trial design innovation. Qualifications: MD or MD/PhD with research training and proven achievement in oncology therapy development; minimum 3 years of clinical drug development experience, including early-phase trials; at least 2 years as a medical monitor in biotech/pharma or CRO. Skills: strong understanding of pharmacokinetics, biomarkers, regulatory requirements, and clinical science; excellent stakeholder engagement, communication, and leadership abilities. High-Value: oncology, immuno-oncology, early to late-phase clinical trials, global regulatory interactions, biomarker strategies, and cross-functional collaboration. Work Setup: flexible US or UK locations; specific arrangements not detailed, likely hybrid or remote.