Medical Director, Clinical Development (Neurology)

Role: Medical Director leading clinical development for one or more early or late-stage oncology or rare disease assets, with a focus on strategic planning, trial oversight, and cross-functional collaboration. Responsibilities: serve as medical monitor, contribute to trial design and data review, author clinical and regulatory documents, develop relationships with key opinion leaders, and support scientific dissemination. Additional duties include mentorship, participating in advisory boards, and supporting business development and continuous improvement initiatives. Requirements: MD or equivalent with 8+ years of relevant academic and industry experience, including 3+ years in clinical trials; expertise in trial design, GCP/ICH, and regulatory compliance; proficiency with data review tools; excellent leadership, communication, and collaboration skills; willingness to travel up to 30%. Preferred qualifications include board certification in neurology, experience in phase 3 trials, and interactions with FDA/regulatory agencies outside the US. High-value biopharma specifics: oncology/rare disease focus, advanced GIST and TGCT indications, involvement in clinical trial phases 1-3, and cross-functional engagement with clinical science, regulatory, and medical affairs teams. Work setup: not specified; travel up to 30%.