Medical Director, Oncology Clinical Development (Solid Tumors)

Role: Clinical Scientist overseeing design, execution, and interpretation of clinical trials in support of AbbVie's therapeutic areas, primarily immunology, oncology, or neuroscience. Objectives include generating high-quality clinical data aligned with product development and regulatory strategies. Responsibilities encompass study protocol development, study oversight (safety, efficacy, enrollment, timelines), data analysis, and cross-functional collaboration, including interactions with opinion leaders and regulatory bodies. Requirements: Medical Doctor (MD, DO, or equivalent), preferably with residency and subspecialty training; ability to independently manage clinical studies; industry or academic trial experience preferred; knowledge of trial methodology, regulatory standards, and Good Clinical Practice (GCP); strong communication skills. High-Value: Therapeutic expertise in immunology, oncology, or neuroscience; experience in early to late-phase trials; familiarity with global regulatory requirements; contribution to regulatory responses; adherence to GCP, pharmacovigilance, and quality standards. Work setup: unspecified; collaboration with medical, regulatory, and operational teams.