Senior Supervising Radiologist

This is a fully remote position, open to applicants in United States, +3 more locations.

📋 Description

• Offer senior leadership in medical and radiology for sponsor studies, which encompasses imaging strategy, protocol development, imaging manuals, reading methodologies, charters, system specifications, training materials, quality assurance, and independent review processes.

• Collaborate with Business Development and operational teams on new business initiatives, bid defenses, capability meetings, and the development of client relationships.

• Represent ICON’s medical, scientific, and imaging expertise in both internal and external discussions.

• Assist in responding to requests for proposals and inquiries by providing scientific, medical, and technical insights.

• Provide immediate consultation on imaging-related scientific and operational inquiries, including protocol formulation, radiology case evaluations, contrast application, imaging analysis, reading design, criteria for readings, and issue resolution.

• Establish trusted client relationships by advising on imaging strategies and supporting responses to regulatory authorities.

• Oversee independent reading teams, which includes reader training, Q&A sessions, performance monitoring, assessment of inter-reader variability, retraining plans, and oversight of reading quality.

• Manage imaging interpretations and offer medical reviews and guidance.

• Engage in industry forums, imaging standardization initiatives, scientific meetings, and external presentations.

• Mentor medical, scientific, and operational colleagues.

• Lead, inspire, and provide guidance to project and study teams.

• Direct medical and scientific activities to ensure timely, comprehensive, and client-oriented delivery.

• Enhance capabilities among medical, scientific, and operational teams by simplifying complex concepts into actionable study guidance.

⛳️ Requirements

• An MD with fellowship training in radiology is mandatory.

• Additional training or proven experience in supporting clinical research is highly preferred.

• Expertise in neuroradiology and body imaging is strongly favored.

• Cross-certification in nuclear medicine is preferred.

• Extensive knowledge of imaging endpoints for clinical trials.

• In-depth understanding of drug development, biomarker development, adaptive design, regulatory submissions, and post-marketing studies.

• Strong familiarity with relevant regulatory expectations, including ICH-GCP and pertinent regional requirements.

• Proven ability to lead complex, large-scale projects and effectively influence through scientific credibility, sound judgment, and stakeholder engagement.

• Exceptional communication and presentation skills.

• Capability to advise clients, support business development initiatives, and represent ICON in public or scientific settings.

• Must reside in the US, UK, or Ireland.

• Willingness to travel up to 10%.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.