AVEO Oncology
JOB TITLE:
Director of Clinical Oncology This role is on-site, Boston (Seaport). JOB SUMMARY: AVEO Oncology is looking for an accomplished Director of Clinical Oncology to be a vital part of our innovative team. The ideal candidate will bring a robust background in oncology, particularly in renal cancer, along with strong experience in early phase clinical development. A proven history in managing global clinical trials is essential for this role, which plays a critical part in advancing our oncology pipeline and executing our clinical programs effectively. PRINCIPAL DUTIES: Demonstrate medical and scientific leadership in designing, executing, and interpreting Phase I clinical studies. Work collaboratively within cross-functional teams including clinical operations, regulatory affairs, and biostatistics to ensure alignment on clinical strategy and study execution. Ensure conducted clinical trials adhere to all applicable regulations, guidelines, and internal policies. Oversee and maintain clinical consistency and quality across all global studies. Lead collaborations with key opinion leaders to shape clinical development plans. Act as medical monitor for clinical trials, providing ongoing oversight and guidance, while addressing challenges to ensure studies are completed timely with high-quality data. Analyze and interpret clinical trial data to guarantee the accuracy and completeness of safety and efficacy details. Partner with pharmacovigilance to monitor and resolve safety concerns and adverse events. Engage in data analysis, interpreting, and presenting clinical study outcomes to both internal and external stakeholders. Assist in the development of clinical study reports, regulatory submissions, and scientific publications. Present findings at scientific conferences and advisory boards to illustrate our progress. Forge and sustain robust relationships with key opinion leaders, investigators, and clinical trial sites. Represent AVEO Oncology at industry events, scientific meetings, and conferences. REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS): Education: MD (Medical Doctor) degree is required. Experience: A minimum of 3-5 years in oncology clinical development, with a focus on Phase I and II clinical studies. Experience managing global clinical trials and adeptness in navigating international regulatory environments is vital. Skills: Strong clinical and scientific expertise in oncology. Exceptional leadership, communication, and interpersonal skills. Proven capability to work effectively within global, cross-functional teams. Strong analytical skills combined with a detail-oriented problem-solving approach. Preferred Qualifications: Background in a biotechnology or pharmaceutical company. Demonstrated success in driving clinical development strategies with data-informed decision-making. Experience engaging with global regulatory bodies and key opinion leaders. Specific experience in renal oncology clinical trials. About AVEO AVEO is a forward-looking, oncology-focused biopharmaceutical company dedicated to delivering meaningful therapies for patients battling cancer. We currently market FOTIVDA (tivozanib) in the U.S. for adults with relapsed or refractory renal cell carcinoma (RCC) post two or more systemic therapies. Our ongoing commitment includes the development of FOTIVDA in various immuno-oncology combinations for RCC and additional indications, along with numerous investigational programs in clinical development. We embrace diversity, equity, and inclusion in our workforce to enhance representation within the company. 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. 2001, 2025 Insperity, under license. All rights reserved.
Director of Clinical Oncology This role is on-site, Boston (Seaport). JOB SUMMARY: AVEO Oncology is looking for an accomplished Director of Clinical Oncology to be a vital part of our innovative team. The ideal candidate will bring a robust background in oncology, particularly in renal cancer, along with strong experience in early phase clinical development. A proven history in managing global clinical trials is essential for this role, which plays a critical part in advancing our oncology pipeline and executing our clinical programs effectively. PRINCIPAL DUTIES: Demonstrate medical and scientific leadership in designing, executing, and interpreting Phase I clinical studies. Work collaboratively within cross-functional teams including clinical operations, regulatory affairs, and biostatistics to ensure alignment on clinical strategy and study execution. Ensure conducted clinical trials adhere to all applicable regulations, guidelines, and internal policies. Oversee and maintain clinical consistency and quality across all global studies. Lead collaborations with key opinion leaders to shape clinical development plans. Act as medical monitor for clinical trials, providing ongoing oversight and guidance, while addressing challenges to ensure studies are completed timely with high-quality data. Analyze and interpret clinical trial data to guarantee the accuracy and completeness of safety and efficacy details. Partner with pharmacovigilance to monitor and resolve safety concerns and adverse events. Engage in data analysis, interpreting, and presenting clinical study outcomes to both internal and external stakeholders. Assist in the development of clinical study reports, regulatory submissions, and scientific publications. Present findings at scientific conferences and advisory boards to illustrate our progress. Forge and sustain robust relationships with key opinion leaders, investigators, and clinical trial sites. Represent AVEO Oncology at industry events, scientific meetings, and conferences. REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS): Education: MD (Medical Doctor) degree is required. Experience: A minimum of 3-5 years in oncology clinical development, with a focus on Phase I and II clinical studies. Experience managing global clinical trials and adeptness in navigating international regulatory environments is vital. Skills: Strong clinical and scientific expertise in oncology. Exceptional leadership, communication, and interpersonal skills. Proven capability to work effectively within global, cross-functional teams. Strong analytical skills combined with a detail-oriented problem-solving approach. Preferred Qualifications: Background in a biotechnology or pharmaceutical company. Demonstrated success in driving clinical development strategies with data-informed decision-making. Experience engaging with global regulatory bodies and key opinion leaders. Specific experience in renal oncology clinical trials. About AVEO AVEO is a forward-looking, oncology-focused biopharmaceutical company dedicated to delivering meaningful therapies for patients battling cancer. We currently market FOTIVDA (tivozanib) in the U.S. for adults with relapsed or refractory renal cell carcinoma (RCC) post two or more systemic therapies. Our ongoing commitment includes the development of FOTIVDA in various immuno-oncology combinations for RCC and additional indications, along with numerous investigational programs in clinical development. We embrace diversity, equity, and inclusion in our workforce to enhance representation within the company. 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. 2001, 2025 Insperity, under license. All rights reserved.