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 clinical trial planning and compliance, ensure data integrity, oversee safety reporting, contribute to regulatory submissions, and provide scientific expertise on molecules and disease areas. May lead or supervise medical/scientific staff, participate in cross-functional teams like Clinical Strategy Teams, and engage with external stakeholders including opinion leaders. Requirements: MD or DO with at least 2 years of clinical trial experience, strong knowledge of trial methodology, regulatory standards, and Good Clinical Practice, plus excellent communication skills. High-Value: focus on immunology, oncology, or neuroscience, with involvement in clinical trials from late preclinical through Phases 1-3; responsibilities include regulatory interactions, study oversight, and cross-functional collaboration. WorkSetup: not specified; likely hybrid or onsite given leadership nature, with international trial oversight.