Medical Director, Oncology Clinical Development (Solid Tumors)

Role: Support clinical development as a supervised clinical research physician, overseeing study design, implementation, and data interpretation to advance AbbVie's therapeutic programs. Responsibilities include designing protocols aligned with regulatory standards, monitoring study integrity, safety, and efficacy data, managing enrollment timelines, and contributing to regulatory documents and scientific reports. The role involves cross-functional collaboration with Medical Affairs, Clinical Operations, and external stakeholders, including opinion leaders, to support therapeutic areas such as immunology, oncology, and neuroscience. The incumbent participates in developing clinical strategies and ensures compliance with GxP, pharmacovigilance, and regulatory requirements. Qualifications: MD or DO with relevant therapeutic specialty, preferably with residency and subspecialty training; prior clinical trial experience in industry or academia; knowledge of trial methodology, regulatory standards, and protocol design; excellent communication skills. Preferred: experience in global drug development, regulatory interactions, and cross-functional teamwork. High-value specifics: involvement in late-phase clinical trials, with a focus on scientifically rigorous data generation supporting product development; regulatory compliance; and contribution to cross-disciplinary teams in a global setting. Work setup: not explicitly stated; likely office-based or hybrid based on industry norms.