Medical Director

JOB TITLE: Medical Director, Oncology Dept: Clinical Development REPORTS TO: Senior Vice President, Head of Clinical Development Location: Boston, MA JOB SUMMARY AVEO Oncology is seeking a highly skilled and experienced Medical Director with a strong background in oncology, specifically renal cancer, and prior experience in early‑phase development. The role involves managing global clinical trials and driving the clinical development of our oncology pipeline. PRINCIPAL DUTIES 1. Leadership skills: Provide medical and scientific leadership in the design, execution, and interpretation of Phase I clinical studies. Collaborate with cross‑functional teams to ensure alignment on clinical strategy and study design. Ensure trials comply with regulations, guidelines, and company policies. Oversee clinical aspects of global studies, maintaining consistency and quality across regions. Lead interactions with key opinion leaders to align clinical development plans. 2. Medical Monitoring and Safety Oversight: Serve as the medical monitor for assigned trials, providing ongoing oversight and guidance. Assess and interpret trial data for accurate safety and efficacy information. Collaborate with pharmacovigilance teams to manage adverse events and safety concerns. 3. Data Analysis and Reporting: Participate in data analysis, interpretation, and presentation of study results. Contribute to preparation of clinical reports, regulatory submissions, and scientific publications. Present clinical data at scientific conferences and advisory boards. 4. Stakeholder Engagement: Develop and maintain relationships with key opinion leaders, investigators, and trial sites. Represent AVEO at scientific meetings, conferences, and industry events. REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS) Education: Medical Doctor (MD) degree is required. Experience: Minimum 3‑5 years in oncology clinical development with familiarity with Phase I and II studies. Experience managing global trials and navigating international regulatory environments. Skills: Strong clinical and scientific acumen in oncology. Excellent leadership, communication, and interpersonal skills. Ability to work effectively in a cross‑functional, global team environment. Strong analytical and problem‑solving skills with attention to detail. Preferred Qualifications: Experience in a biotechnology or pharmaceutical company. Track record driving clinical development strategies and making data‑driven decisions. Experience interacting with global regulatory agencies and key opinion leaders. Experience in renal oncology clinical trials. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. #J-18808-Ljbffr