Medical Director, Oncology Clinical Development (Solid Tumors)

Role: Clinical Research Physician supporting AbbVie's clinical development programs in immunology, oncology, or neuroscience. Responsibilities include designing and implementing study protocols, overseeing study conduct, monitoring data safety and efficacy, and ensuring compliance with regulatory standards. Contributes to scientific documentation, participates in cross-functional clinical strategy teams, and engages with opinion leaders. Maintains knowledge of therapeutic areas and regulatory requirements to support global drug development efforts. Qualifications: Medical Doctor (MD or DO) or equivalent with relevant specialty, preferably with residency and fellowship training; clinical trial experience in industry, academia, or similar setting; strong understanding of trial methodology, regulatory guidelines, and GxP standards; excellent communication skills in English. HighValue: focus on early to late-stage clinical trials, compliance with GCP, involvement in cross-functional teams including Medical Affairs and Regulatory, and therapeutic areas such as immunology, oncology, or neuroscience. Work setup: not specified, but likely office-based with potential cross-functional collaboration.