Senior Medical Director, Oncology Clinical Development (GI)

Role: Lead clinical development activities for AbbVie's therapeutic programs, overseeing trial design, execution, and data interpretation to support product strategies. Responsibilities: manage multi-phase clinical trials, ensure study integrity, oversee safety monitoring, and contribute to regulatory submissions. Lead scientific content creation for protocols, reports, and submissions; collaborate with cross-functional teams including Medical Affairs and Discovery. Qualifications: MD or DO with at least 2 years of clinical trial experience, strong knowledge of trial methodology, regulatory compliance, and GxP standards. Preferred: subspecialty training and experience in immunology, oncology, or neuroscience, with capability to lead global clinical programs. High-Value: involved in early to late-stage clinical trials, responsible for regulatory interactions, adherence to GCP, and understanding of global drug development processes. Work Setup: location unspecified; the role likely involves cross-functional collaboration and oversight of multiple study sites.