Physician

• 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 on new business opportunities, bid defenses, capabilities meetings and client relationship development
• Represent ICON’s medical, scientific and imaging expertise in internal and external discussions
• Support responses to requests for proposals and information with scientific, medical and technical input
• Provide real-time consultation on imaging-related scientific and operational questions, including protocol development, radiology case review, contrast use, imaging analysis, read design, read criteria and issue resolution
• Build trusted client relationships by advising on imaging strategy and supporting regulatory authority responses
• Supervise independent read teams, including reader training, Q&A, performance monitoring, inter-reader variability assessment, retraining plans and read-quality oversight
• Oversee imaging reads and provide medical review and guidance
• Participate in industry forums, imaging standardization initiatives, scientific meetings and external presentations
• Mentor medical, scientific and operational colleagues
• Lead, motivate and advise project and study teams
• Guide medical and scientific activities for timely, complete and client-focused delivery
• Develop capability across medical, scientific and operations teams by translating complex concepts into practical study guidance

Senior Supervising Radiologist

• Provide senior clinical leadership across assigned trials, ensuring participant safety, protocol compliance, and data integrity throughout the study lifecycle
• Act as Principal Investigator or Sub-Investigator as required, taking accountability for medical decision-making and oversight within delegated studies
• Provide leadership, supervision, and mentorship to Research Physicians and wider site teams
• Lead or contribute to feasibility assessments, protocol reviews, and study start-up planning
• Contribute to business development, sponsor engagement, proposals, bid responses, business cases, and service development initiatives
• Review study budgets, contracts, and resource requirements from a medical and operational perspective
• Maintain senior oversight of ICH-GCP, regulatory requirements, ethical standards, and sponsor protocols
• Lead or support investigations into protocol deviations, safety events, and quality concerns, including documentation, escalation, and corrective actions
• Support and represent EMS Healthcare during audits, inspections, and regulatory reviews
• Provide expert clinical guidance to Principal Investigators, Research Physicians, and multidisciplinary study teams
• Contribute to training, induction, and ongoing research capability development
• Develop and maintain sponsor and client relationships as a senior medical contact
• Build working relationships with regulatory authorities, ethics committees, investigators, and senior internal stakeholders
• Collaborate with the EMS Healthcare Medical Advisory Committee and cross-functional leaders
• Provide senior medical oversight across multiple studies and research sites
• Oversee clinical trial delivery across community-based and mobile research settings
• Contribute to clinical and operational protocols, SOPs, and quality systems
• Represent the medical function at sponsor, client, and cross-functional meetings

Senior Research Physician

• Support the Principal Investigator team in executing clinical trials, ensuring participant safety, protocol adherence, and data integrity
• Act as a Principal Investigator for designated trials under senior PI guidance
• Assist with competency checks and staff reviews, ensuring required training and certifications are current
• Participate in trial feasibility assessments and protocol reviews
• Collaborate with sponsors and internal teams to assess site capabilities and study requirements
• Identify research opportunities and assist with proposals and business cases
• Support review of trial costs and contracts
• Ensure compliance with ICH-GCP, regulatory and ethical standards, and sponsor protocols
• Support internal and external audits, inspections, and regulatory reviews
• Stay current on clinical trial developments and best practices
• Provide clinical and operational support to Principal Investigators and research teams
• Develop as a mentor to guide junior staff and support consistent trial delivery
• Communicate with sponsors, regulatory authorities, and ethics committees
• Collaborate with internal teams, including the EMS Healthcare Medical Advisory Committee, to improve service delivery
• Help ensure smooth clinical trial operations across community-based research sites, including recruitment and study coordination
• Contribute to EMS Healthcare’s operational protocols and quality systems
• Attend sponsor and client meetings as required