Clinical Imaging Scientific Director – Oncology

🔥 0 minutes ago

🏖️ New Jersey, New York, +1 more states – Remote

🏖️ New Jersey – Remote 🗽 New York – Remote 🍂 Massachusetts – Remote

💵 $205k - $341.6k / year

⏰ Full Time

🔴 Lead

👔 Director

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Regeneron

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1988

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 Post-IPO Equity on 2023-10

Healthcare • Manufacturing • Biotechnology

Regeneron is a biotechnology company dedicated to turning scientific discoveries into life-changing medicines. The company focuses on a range of serious diseases including allergic, cardiovascular, and metabolic diseases, neuroscience, oncology, hematology, ophthalmology, and rare diseases. It achieves this by integrating biology and technology to develop cutting-edge biologics and genetic medicines. Regeneron is committed to health equity, environmental sustainability, and supporting future STEM talent through initiatives like the Regeneron Science Talent Search. By maintaining high ethical standards and corporate responsibility, Regeneron aims to push the boundaries of science for better healthcare solutions.

📋 Description

• Own the strategy and execution of sophisticated early- and late-phase oncology imaging in clinical trials • Develop imaging endpoints and biomarkers and drive scientific imaging and tumor response assessment for oncology clinical studies • Create fit-for-purpose imaging biomarker strategies with research, clinical imaging and oncology therapeutic-area teams • Prepare and present clinical imaging strategies to senior management • Manage a complex network of stakeholders across Regeneron • Lead, design and implement multi-modality imaging measures as endpoints for oncology clinical studies • Collaborate with clinical teams as the imaging subject matter expert on imaging strategies, protocols, endpoints, manuals, charters, statistical analysis plans and clinical study reports • Work with Clinical Imaging Operations and imaging contract research organizations to ensure study imaging components and endpoint data integrity • Serve as Study Scientific Director for clinical trials qualifying and utilizing novel imaging biomarkers • Lead regulatory-agency interactions regarding imaging endpoints, procedures and biomarker development studies • Lead interactions with regulatory agencies and site ethics committees for approval of clinical imaging biomarker development studies

🎯 Requirements

• PhD program with a minimum of 10+ years of clinical imaging experience, including a minimum of 7 years within oncology drug development • Superior written and verbal communication and organization skills • Experience implementing central efficacy assessments using RECIST 1.1, iRECIST, PCWG3, Lugano and IMWG in oncology clinical trials • Successful engagement experience with regulatory agencies • Ability to champion imaging innovations and lead projects effectively • Experience as study scientific director of PET imaging biomarker clinical trials in Oncology • Experience applying PET imaging as a quantitative endpoint in clinical and preclinical studies in Oncology

🏖️ Benefits

• Annual bonuses or other incentive plans • Equity awards • Pension or retirement benefits • 401(k) company match • Health and wellness programs • Fitness centers • Medical, dental, vision, life and disability insurance benefits • Paid time off • Family support benefits • Reasonable accommodation during the recruitment process for applicants with known disabilities or chronic illnesses