The Clinical Scientist Director - Late Development Oncology, is a key member of the clinical development team, supporting the execution of oncology clinical trials through protocol oversight, medical data review, and clinical data quality activities. The role ensures studies are conducted in accordance with protocol requirements, regulatory expectations, and company quality standards.Main responsibilities include acting as a scientific and clinical subject matter expert, supporting medical monitoring activities, assessing clinical data to identify trends and risks, and ensuring the generation of accurate and reliable data for decision making. The position collaborates closely with cross functional teams, external partners, consultants, and Clinical Research Organizations to support successful study delivery.The role contributes to the development and review of study concepts, protocols, and related documentation, supports implementation of clinical trials, reviews and analyzes clinical data, and assists with interpretation of study results. Additional responsibilities include data quality assessments, adherence to Good Clinical Practice requirements, and maintaining data integrity throughout the clinical trial lifecycle.The ideal candidate has experience in pharmaceutical clinical development, particularly in oncology, with knowledge of clinical trial design, monitoring, execution, and regulatory requirements. Experience with data review, submission documentation, scientific publications, conference presentations, and clinical data analysis tools is highly valued.Success in this role requires strong scientific, analytical, communication, problem solving, and collaboration skills, as well as the ability to work effectively across multidisciplinary teams and support the development of innovative treatments for patients.