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

Role: Lead and oversee clinical development programs for AbbVie's therapeutic areas, focusing on designing, implementing, and interpreting complex clinical trials. Objectives include generating high-quality clinical data to support product strategy and regulatory approval. Responsibilities encompass leading cross-functional teams, ensuring study integrity, managing timelines and enrollment, and preparing scientific and regulatory documents such as protocols and reports. May serve as a clinical expert for disease areas like hematology or lymphoma, contributing to scientific discussions, due diligence, and translational strategies. Requirements include a Bachelor's degree in sciences (advanced degree preferred), at least 8 years of clinical trial experience in pharma or academia, with expertise in hematology/NHL preferred. Proven leadership skills, ability to manage complex programs independently, and deep knowledge of clinical methodologies, regulatory standards, and GxP compliance are essential. The role involves collaboration with Medical Affairs, Commercial, Regulatory, and Discovery teams, representing AbbVie externally at scientific meetings. The position requires staying current with therapeutic advances and regulatory requirements, with a focus on global drug development. This role is based in the US, with no explicit travel requirements stated.