The Clinical Scientist Director supports early phase oncology clinical development by translating scientific and clinical strategy into the execution of clinical trials. As a key member of cross-functional clinical development teams, the role provides scientific and clinical expertise to ensure high-quality study execution, protocol compliance, regulatory alignment, and data integrity.Key responsibilities include supporting protocol development and governance, contributing to medical monitoring activities, reviewing subject level clinical data, identifying risks and trends, and ensuring clinical trials generate accurate, complete, and decision-ready data. The position collaborates closely with internal teams, external partners, consultants, and Clinical Research Organizations to support successful study delivery.The role contributes to the development of study concepts, protocols, and related documents, provides clinical input into trial implementation and data review activities, and supports the interpretation of study results. Responsibilities also include conducting data quality assessments, ensuring adherence to Good Clinical Practice and regulatory requirements, and maintaining high standards of data accuracy throughout the trial lifecycle.The ideal candidate has significant experience in clinical drug development, preferably in oncology and early phase research. Strong knowledge of clinical trial design, monitoring, execution, data review, regulatory submissions, and scientific communications is required. Experience with clinical data analysis tools, scientific publications, conference presentations, and regulatory interactions is highly valued.Success in the role requires excellent scientific, analytical, communication, leadership, and collaboration skills, with the ability to work effectively across multidisciplinary teams and support the delivery of innovative therapies for patients.