Role Description The Insurance Risk Management Analyst supports the Risk Manager regarding corporate insurance programs, insurance certificates, and casualty claims management. - Certificates of Insurance (35%) - Issue certificates of insurance for van line operations, as requests are received. - Secure required information from van line agents, review insurance requirements from third-parties, and issue certificates of insurance in alignment with Sirva insurance policy terms & procedures. - Partner with Risk Manager and Sirva legal, as needed, to respond to indemnity language requests. - Issue certificates of insurance in support of client contractual agreements. - Review the insurance section of the client contract and issue certificates of insurance in alignment with agreed upon contractual insurance terms. - Corporate Risk Insurance Programs (25%) - Assist the Risk Manager in compilation of underwriting information for insurance policy placements, domestic and international. - Activities include analysis of underwriting information for accuracy, timely completion of applications and maintenance and review of insurance policy documents. - Support legal, sales and operations in the review of insurance terms in client contracts and new business proposals. - Manage the surety bond program. Work with surety broker and internal teams on bond issuances, cancellations, reporting and invoicing. - Casualty Claims Management (40%) - Support Sirva safety department, agent network, and van line drivers in investigation and documentation of fleet accidents. - Monitor the development of van line auto and general liability claims, to include tracking claim progress and identifying potential risks. - Collaborate with the TPA claim adjuster and defense counsel on claim strategy for optimal claim resolution. Qualifications - BS degree in risk management, business, or finance. - Property/Casualty Insurance Producer license, preferred. - Experience with commercial insurance placements and oversight, claims management, and/or the risk management function. - Detail-oriented and proficient in Microsoft Excel, Outlook, and Word. Requirements - Salary Range: $66,400 - $83,000 USD. Benefits - Comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Employer HSA Match, Life & Disability Insurance, Paid Time Off, Volunteer Time Off, ID Theft Protection Plan and more. - Benefits are based on employment status and may not be available for temporary or non full-time employees.

• Assist with routine tasks and projects within the risk advisory function. • Support risk assessments, project planning, and execution of work plans. • Help evaluate business processes and IT general controls. • Communicate ideas and findings clearly with team members and clients. • Identify and analyze technical issues, providing recommendations to management. • Adhere to industry regulations and professional ethics, including IIA, ISACA, GAO, and AICPA guidelines. • Assist in managing engagement activities and ensuring quality standards are met. • Maintain awareness of client needs and take initiative in day-to-day tasks. • Support risk management efforts and uphold quality control procedures. • Build and maintain positive client relationships through effective communication. • Respond promptly and accurately to team and client requests. • Adapt to client needs and evolving project requirements. • Seek continuous learning opportunities and ways to improve processes.

Role Description As a Central Monitor at ICON, you will ensure the quality and integrity of clinical trial data through centralized monitoring activities, contributing to the advancement of innovative treatments and therapies. What You Will Do: - Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. - Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality. - Collaborate with site personnel and clinical teams to address findings from centralized monitoring activities and implement corrective and preventive actions as necessary. - Utilize advanced data analytics tools and technology platforms to enhance the efficiency and effectiveness of centralized monitoring processes. - Provide support and guidance to study teams on centralized monitoring methodologies, best practices, and regulatory requirements. - Contribute to the development and optimization of centralized monitoring strategies and protocols to maximize data quality and compliance across clinical trials. Qualifications - Bachelor's degree in life sciences, computer science, or a related discipline. - Previous experience in clinical research, data management, or monitoring within the pharmaceutical, biotechnology, or CRO industry. - Strong understanding of clinical trial processes, regulations, and guidelines (e.g., ICH GCP, FDA regulations). - Excellent analytical and critical thinking skills with the ability to identify patterns, trends, and discrepancies in clinical trial data. - Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and communicate complex concepts to diverse stakeholders. - Willingness to travel as required (approximately 5%). Requirements - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits - Competitive base salary and performance related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. - Benefits may vary depending on role and location.

Role Description As a Clinical Data Risk Analyst - Central Monitor at ICON, you will identify and mitigate risks associated with clinical trial data. You will contribute to the overall success of our clinical programs by employing risk assessment methodologies to ensure data integrity and compliance with regulatory standards. Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include: - Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies. - Collaborating with cross-functional teams to develop and implement risk management plans and protocols. - Monitoring data quality and integrity throughout the trial process, reporting findings to stakeholders. - Utilizing statistical analysis and visualization tools to communicate risk-related insights effectively. - Supporting the preparation of risk management documentation for regulatory submissions and audits. Qualifications - Degree in statistics, life sciences, or a related field. - Experience in clinical data analysis or risk management within a clinical research environment. - Strong analytical skills with proficiency in statistical software and risk assessment methodologies. - Attention to detail and a proactive approach to identifying and addressing data risks. - Effective communication skills, with the ability to collaborate across diverse teams and convey complex information clearly. Requirements - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits - Competitive base salary and performance-related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. - Benefits may vary depending on role and location.