ICON Strategic Solutions
Senior Clinical Research Associate, Remote, Midwest Region
ICON Strategic Solutions, Des Moines, Iowa, United States
Overview
Senior Clinical Research Associate, Remote, Midwest Region ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a Senior Clinical Research Associate (CRA) in the Midwest Region to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. Ideal locations would be:
Kansas City, MO St. Louis, MO Des Moines, IA Wichita, KS Chicago, IL Omaha, NE What You Will Be Doing
Perform site management activities to support Oncology site success and maintain a continuous state of inspection readiness Act as the primary contact and facilitate efficient communications between the clinical trial team and the sites Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in trials May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs Promptly document monitoring activities and submit/approve visit reports Manage site essential document collection and TMF reconciliation with site files Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations Support sites during regulatory inspections Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities Lead site engagement initiatives and foster relationships with key Oncology sites and networks Your Profile
Bachelor’s degree (scientific field preferred) 5+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits 1+ years early development trial experience preferred Solid tumor clinical trial experience is preferred Experience utilizing Veeva CTMS for report writing is required Demonstrated experience developing/maintaining site relationships and securing compliance Expertise in GCPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology Experience collaborating with sites from initial engagement through close-out phases Experience activating sites Experience training site staff Experience supporting sites and/or sponsors in regulatory inspections Experience working within an FSP (or in-house) monitoring model is preferred Willing to travel up to 50% domestically Reside in Midwest Region USA 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 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. ICON is committed to inclusion and belonging. We provide an inclusive and accessible environment for all candidates. 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 you need a reasonable accommodation for any part of the application process, please let us know. Interested in the role? We encourage you to apply regardless—even if you don’t meet every requirement.
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Senior Clinical Research Associate, Remote, Midwest Region ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a Senior Clinical Research Associate (CRA) in the Midwest Region to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. Ideal locations would be:
Kansas City, MO St. Louis, MO Des Moines, IA Wichita, KS Chicago, IL Omaha, NE What You Will Be Doing
Perform site management activities to support Oncology site success and maintain a continuous state of inspection readiness Act as the primary contact and facilitate efficient communications between the clinical trial team and the sites Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in trials May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs Promptly document monitoring activities and submit/approve visit reports Manage site essential document collection and TMF reconciliation with site files Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations Support sites during regulatory inspections Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities Lead site engagement initiatives and foster relationships with key Oncology sites and networks Your Profile
Bachelor’s degree (scientific field preferred) 5+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits 1+ years early development trial experience preferred Solid tumor clinical trial experience is preferred Experience utilizing Veeva CTMS for report writing is required Demonstrated experience developing/maintaining site relationships and securing compliance Expertise in GCPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology Experience collaborating with sites from initial engagement through close-out phases Experience activating sites Experience training site staff Experience supporting sites and/or sponsors in regulatory inspections Experience working within an FSP (or in-house) monitoring model is preferred Willing to travel up to 50% domestically Reside in Midwest Region USA 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 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. ICON is committed to inclusion and belonging. We provide an inclusive and accessible environment for all candidates. 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 you need a reasonable accommodation for any part of the application process, please let us know. Interested in the role? We encourage you to apply regardless—even if you don’t meet every requirement.
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