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.
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 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.
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.
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
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.
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
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.
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.
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.
Hybrid · Mississauga
Coordinate and administer clinical trials in compliance with study protocols and regulatory requirements, while maintaining study files, essential documents, and regulatory submissions. Prepare study materials, collaborate with cross-functional teams, and track and report trial metrics and milestones.
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.
On-site
Coordinate and oversee oncology clinical trial activities, ensuring compliance with protocols and regulatory requirements, data integrity, quality, and project timelines. Collaborate with study teams, investigators, and sites, support clinical staff, track progress, and identify and mitigate risks.
On-site
The Study Start-up Specialist will lead and support clinical trial activation activities, including regulatory submissions and site maintenance. They will manage essential clinical trial documentation and ensure compliance with ICH-GCP and FDA requirements.
On-site
The Site Activation Partner facilitates clinical trial initiation by managing regulatory submissions and coordinating with stakeholders to obtain necessary approvals. They also support study teams in developing essential documentation such as protocols and informed consent forms.
