As Director, Medical & Scientific Affairs, Oncology, you will serve as a strategic scientific leader supporting global clinical trials, client partnerships, operational excellence, and product innovation. This role combines therapeutic expertise, leadership, and business acumen to help deliver high-quality imaging solutions that advance clinical research and improve patient outcomes. If you are passionate about driving scientific innovation and influencing the future of imaging in clinical trials, we encourage you to apply.
What We Offer- Competitive compensation
- Medical, dental, and vision coverage
- Paid time off
- Employee assistance and wellness programs
- Life and disability insurance
What You'll Be Doing- Partner with Business Development to support new business opportunities, client engagements, proposal development, bid defense activities, and market expansion initiatives.
- Serve as a scientific and technical consultant for clients, providing expertise in imaging strategy, trial design, image review methodology, and quality control throughout the lifecycle of clinical studies.
- Lead the development, review, and execution of imaging-related study documentation, including imaging charters, manuals, read rules, reports, and study-specific operational requirements.
- Provide medical and scientific guidance to cross-functional teams to ensure the successful delivery of imaging services for ongoing clinical trials.
- Drive innovation by identifying new imaging methods, technologies, tools, and service offerings that enhance operational effectiveness and client value.
- Support product development initiatives by gathering scientific requirements and providing input on software enhancements, new features, and technology roadmaps.
- Monitor operational and delivery metrics, identify process improvements, and implement strategies that improve quality, efficiency, and scalability.
- Build strong relationships with clients, investigators, key opinion leaders, and industry stakeholders while representing Clario, a part of Thermo Fisher Scientific at scientific meetings and conferences.
- Lead training and development efforts across departments, ensuring teams maintain expertise in therapeutic area requirements, imaging methodologies, and operational best practices.
- Support reader identification, qualification, training, and performance monitoring activities across assigned studies.
- Collaborate with senior leadership to develop operational strategies, establish departmental priorities, and support financial forecasting and resource planning.
- Ensure the scientific integrity, quality, and timely delivery of all project deliverables while contributing to continuous improvement initiatives across the organization.
What We Look For- Bachelor's degree in a scientific, clinical, technical, or related discipline; advanced degree (M.S., Ph.D., or M.D.) preferred.
- 10+ years of clinical trial experience within a contract research organization (CRO), pharmaceutical company, or related clinical research environment.
- Experience working within regulated environments, including Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, FDA regulations, ISO standards, or 21 CFR Part 11 requirements.
- Proven leadership experience managing teams, coaching employees, and driving cross-functional collaboration.
- Strong understanding of clinical research, imaging operations, project management, and data management processes.
- Demonstrated expertise in imaging methodologies, image review processes, and therapeutic-area-specific clinical trial applications.
- Experience supporting client-facing activities, including proposal development, scientific consultations, presentations, and governance meetings.
- Strong analytical, organizational, and documentation skills with exceptional attention to detail.
- Excellent written, verbal, presentation, and stakeholder communication skills.
- Proven ability to influence decision-making, lead strategic initiatives, and manage multiple priorities in a fast-paced environment.
- Proficiency with Microsoft Office applications, including Word and Excel.
- Demonstrated publication history and directly relevant scientific research experience preferred.
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