ICON Strategic Solutions is the global leading provider of Functional Service Provision (FSP) services. Through combined functional, operational, and talent expertise, ICON offers FSP models that provide cost-savings, clinical expertise and significantly improve business performance. Follow us for the latest industry insights as well as vacancies and insight into life at ICON.
On-site
Conduct assigned site qualification, initiation, monitoring, and closeout activities while verifying protocol, GCP, and regulatory compliance and protecting trial participants. Review source data, essential documents, and site processes; follow up on findings and risks; and communicate with investigators, site staff, and study teams.
Remote · Canada
Conduct qualification, initiation, monitoring, and close-out visits at clinical trial sites while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, review clinical data and resolve queries, and contribute to study documentation, including protocols and clinical study reports.
Hybrid · Kirkland
Coordinate clinical trial and site administration, including essential documents, clinical databases, supplies, regulatory submissions, and electronic trial master file quality control. Support country and site budgets, contract negotiations, investigator and vendor payments, financial compliance, and local investigator meetings.
On-site
Build and maintain relationships with clinical trial site stakeholders, and guide site staff on study protocols, procedures, and regulatory requirements. Improve and monitor site engagement and performance, collaborate with internal teams on tailored strategies, and report engagement outcomes to study teams.
On-site
Oversee site-level clinical trial administration, including meeting coordination, document management, data entry, and support for investigator engagement. Assist with participant retention and enrollment, troubleshoot study platforms, prepare site reports, and coordinate site visits and related requests.
Remote · Canada, United States
Lead the scientific and clinical execution of global oncology studies, including study design, medical monitoring, safety oversight, data review, and collaboration with investigators and cross-functional teams. Contribute to regulatory submissions, clinical study reports, publications, and study training, while mentoring junior clinical scientists as needed.
On-site
Oversee and provide administrative support for clinical trial site activities, including document management, data entry, meeting coordination, and investigator engagement. Support participant retention and enrollment, troubleshoot clinical trial platforms, prepare site reports, and coordinate site visit requests.
On-site
Lead complex programs from planning through delivery, managing timelines, budgets, resources, and cross-functional teams to meet business objectives. Oversee site resourcing and workforce planning, communicate progress and risks to stakeholders, and implement process improvements.
On-site
Prepare and submit regulatory documents, coordinate approvals with internal and external stakeholders, and maintain accurate records of submissions and authorizations. Support study teams with study documents and contribute regulatory guidance and timelines during start-up meetings.
Remote · Canada
Conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, review clinical data and resolve queries, and contribute to study documentation, protocols, and clinical study reports.
On-site
Monitor clinical trial sites and conduct site visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice, while resolving issues and supporting trial execution. Collaborate with cross-functional teams, support accurate and timely data collection and reporting, and train site staff and other CRAs.
On-site
Conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, review clinical data and resolve queries, and contribute to study documentation, protocols, and clinical study reports.
On-site
Monitor clinical trial sites and conduct site visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice, while assessing site performance and resolving operational issues. Coordinate with cross-functional teams, support accurate and timely data collection and reporting, train site staff and other CRAs, and maintain effective stakeholder relationships.
On-site
Monitor clinical trial sites and conduct site visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice, while assessing site performance and resolving operational issues. Coordinate with cross-functional teams to support accurate, timely data collection and reporting, and train site staff and other CRAs to promote quality and effective trial operations.
On-site
Monitor clinical trial sites and conduct site visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice, while assessing site performance and resolving operational issues. Coordinate with cross-functional teams, support accurate and timely data collection and reporting, train site staff and other CRAs, and maintain effective stakeholder relationships.
Remote · Canada
Monitor clinical trial sites and conduct site visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice standards. Coordinate with cross-functional teams, support site staff and other CRAs, and maintain effective stakeholder relationships to promote accurate, timely, and high-quality trial execution.
On-site
Own site start-up activities from initiation through activation, ensuring regulatory requirements are met. Prepare and coordinate regulatory submissions and approvals, maintain accurate records, and support the development and review of study documents.
Remote · Canada
Lead country-level study start-up and site activation, including preparing, reviewing, tracking, and submitting regulatory and essential site documents in compliance with ICH-GCP, client procedures, and local requirements. Coordinate with study teams and sites, maintain study systems and performance metrics, resolve outstanding actions, and support quality checks to ensure sites are ready to enroll on schedule.
On-site
Prepare and submit regulatory and ethics documents, coordinate approvals and authorizations, and maintain accurate records for clinical study start-up and site activation. Support study teams with study documents and contribute to start-up meetings by advising on regulatory requirements and timelines.
Remote · Canada
Coordinate and oversee oncology clinical trial activities, ensuring compliance with protocols and regulatory requirements, data integrity, quality, and project timelines. Collaborate with study teams, sites, investigators, and clinical staff to resolve issues, monitor progress, mitigate risks, and improve trial execution.
