Scientific Director I, Oncology Early Development

Role: Lead clinical development activities within AbbVie's hematology, oncology, or cell therapy programs, overseeing trial design, execution, and data interpretation. Responsibilities include managing 1-2 clinical studies, ensuring study integrity and data quality, and developing clinical protocols and regulatory documents. The role involves cross-functional collaboration with Medical Affairs, Discovery, and external stakeholders, as well as oversight of CROs and vendors. The incumbent participates in asset strategy and regulatory discussions, staying current with scientific advancements. Qualifications: Bachelor's in sciences, advanced degree preferred; 5+ years of clinical trial experience in pharma or academia. Skills include trial methodology, regulatory compliance, and study protocol development. High-Value: Focus on hematology, oncology, or cell therapy, supporting global drug development, with responsibilities spanning GxP adherence, regulatory interactions, and cross-functional team leadership. Work setup and travel details are not specified.