Senior Supervising Radiologist

ICON; Center Square (PA); Remote; USD 180,000 - 240,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme (

Job summary

ICON seeks a Senior Supervising Radiologist to provide senior medical, scientific and radiological leadership for imaging strategy and oversight across global clinical trials.

You will partner with BD and operations to drive business opportunities, engage with clients, and supervise independent read teams to ensure high-quality image interpretation and regulatory alignment. This is a remote role with travel up to 10% and requires radiology fellowship training and US/UK/Ireland residency.

Qualifications

• MD with fellowship training in radiology required.
• Expertise in neuroradiology and body imaging preferred.
• Cross-certification in nuclear medicine preferred.
• Deep expertise in imaging endpoints for clinical trials with regulatory knowledge.
• Strong knowledge of ICH-GCP and regional requirements.
• Demonstrated ability to lead complex, large-scale projects and influence thru scientific credibility.
• Excellent communication and presentation skills for clients and forums.
• Live in US, UK, or Ireland.
• Ability to travel up to 10%.

Responsibilities

• Provide senior medical and radiology leadership for sponsor studies, including imaging strategy and read methodologies.
• Partner with Business Development and operations for new opportunities and client engagement.
• Represent ICON's imaging expertise in discussions to support study quality and regulatory readiness.
• Support responses to RFPs with scientific and technical input.
• Provide real-time imaging-related consultation to sponsors, sites, and teams.
• Build client relationships by advising on imaging strategy and addressing study-specific issues.
• Supervise independent read teams and ensure read quality and consistency.
• Oversee imaging reads and provide medical review aligned with study requirements.
• Contribute to ICON's scientific credibility through industry forums and meetings.
• Mentor colleagues to strengthen understanding of imaging endpoints and CRO role.
• Lead project teams to deliver high-quality imaging and medical deliverables.
• Guide activities to ensure timely, client-focused delivery across studies.
• Develop capability by translating complex concepts into practical study guidance.

Skills

Neuroradiology

Body imaging

Regulatory knowledge

Leadership

Communication

Stakeholder engagement

Travel readiness

Nuclear medicine

Education

MD with radiology fellowship

Job description

Senior Supervising Radiologist - REMOTE

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Senior Supervising Radiologist to join our diverse and dynamic Medical & Scientific Affairs team within ICON's Medical Imaging group. In this role, you will provide senior medical, scientific and radiological expertise to support imaging strategy, clinical trial delivery, independent reader oversight, business development and client engagement across ICON's global clinical research, outcomes, laboratory and technology services.

What you will be doing

• Provide senior medical and radiology leadership for sponsor studies, including imaging strategy, protocol design, imaging manuals, read methodology, charters, system requirements, training materials, quality control and independent reviewer processes.

• Partner with Business Development and operational teams to support new business opportunities, bid defenses, capabilities meetings and client relationship development through expert medical and scientific input.

• Represent ICON's medical, scientific and imaging expertise in internal and external discussions, making independent recommendations that support study quality, regulatory readiness and client success.

• Support responses to requests for proposals and information by providing scientific, medical and technical input that demonstrates ICON's imaging expertise in clinical trials.

• Provide real-time consultation to internal teams, sponsors, sites and clients on imaging-related scientific and operational questions, including protocol development, radiology case review, contrast use, imaging analysis, read design, application of read criteria and resolution of imaging-related issues.

• Build trusted client relationships by advising on imaging strategy, discussing and resolving study-specific imaging issues, and supporting responses to regulatory authority queries related to study design and radiological assessment.

• Supervise independent read teams, including reader training, ongoing Q&A, performance monitoring, assessment of inter-reader variability, retraining plans and oversight of read quality to support consistent, high-quality image interpretation.

• Oversee imaging reads and provide medical review and guidance to ensure read outputs are clinically appropriate, scientifically sound and aligned with study requirements.

• Contribute to ICON's scientific credibility through participation in industry forums, imaging standardization initiatives, scientific meetings and external presentations.

• Mentor medical, scientific and operational colleagues to strengthen understanding of imaging endpoints, clinical trial objectives and the role of a CRO in drug development.

• Lead, motivate and advise project and study teams to deliver high-quality imaging and medical/scientific deliverables for clients.

• Guide medical and scientific activities to ensure timely, complete and client-focused delivery across assigned studies and programs.

• Develop capability across medical, scientific and operations teams by translating complex clinical, radiological and drug development concepts into practical study guidance.

Your profile

• MD with fellowship training in radiology is required; additional training or demonstrated experience supporting clinical research is strongly preferred.

• Expertise in neuroradiology and body imaging is strongly preferred.

• Cross-certification in nuclear medicine is preferred.

• Deep expertise in imaging endpoints for clinical trials, with comprehensive knowledge of drug development, biomarker development, adaptive design, regulatory submission and post-marketing studies.

• Strong working knowledge of applicable regulatory expectations, including ICH-GCP and relevant regional requirements.

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

• Excellent communication and presentation skills, with the ability to advise clients, support business development activities and represent ICON in public or scientific forums.

• Live in the US, UK, or Ireland

• Ability to travel up to 10%

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here