Senior Scientific Director, Oncology Clinical Development (Non-Hodgkin Lymphoma)

Role: Lead and oversee the design, execution, and interpretation of clinical trials within one or more complex development programs, focusing on therapeutic areas such as immunology, oncology, neuroscience, or eye care. The role involves developing clinical strategies, ensuring compliance with regulatory standards, and managing cross-functional teams, including Medical and Scientific Directors. Responsibilities include leading protocol development, data analysis, regulatory submissions, and contributing to scientific and medical activities, including stakeholder engagement and external representation. The position requires acting as a clinical expert, supporting due diligence, and integrating translational strategies. Qualifications: Bachelor's in sciences with an advanced degree (MS, PhD) preferred; minimum 8 years' experience in clinical research, with expertise in clinical trial methodology, regulatory compliance, and development of clinical strategies. Hematology or Non-Hodgkin Lymphoma experience is highly preferred. Skills required include leadership, cross-functional collaboration, strong communication, and strategic thinking. High-value specifics: experience in late-stage clinical trials, regulatory interactions, and global program oversight in biopharma settings; focus on complex oncology or immunology programs; active engagement with external stakeholders and representation at conferences. Location and travel details are not specified.