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 · Canada
The Study Start Up CRA is responsible for site selection and the execution of start-up activities for Phase I-IV trials. This includes managing regulatory submissions, negotiating investigator payments, and ensuring sites are ready for 'Green Light' approval.
On-site · Canada
Oversee the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies. Coordinate with legal and finance teams to manage contract workstreams and improve cycle times.
On-site · Canada
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Responsibilities include ensuring protocol compliance, maintaining data integrity, and collaborating with investigators to facilitate study conduct.
On-site
Sr. Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies. What You Will Do: You will take…
Remote · Canada
Lead and coordinate country-level clinical study activities from startup through close, ensuring delivery on time, within budget, and to quality standards. Oversee pCROs and local study teams while managing risk mitigation, stakeholder communication, and regulatory compliance.
On-site · Canada
The Local Trial Manager is responsible for end-to-end trial delivery at the country level, serving as the single point of contact for internal partners. Key duties include managing local vendors, executing milestones from feasibility to close-out, and ensuring inspection readiness.
On-site · Canada
Responsible for managing and overseeing country-level study activities from startup through close, including site identification and recruitment. Leads the Local Study Team and ensures compliance with global and local regulatory requirements while managing pCROs and vendors.
Remote · Canada
Responsible for the management and oversight of US clinical trial deliverables from startup through close. This includes managing budgets, vendors, and cross-functional teams while ensuring compliance with global and local regulations.
On-site · Canada
The role involves reviewing, analyzing, and negotiating contracts and legal documents related to clinical trials and vendor relationships. The manager will collaborate with cross-functional teams to mitigate risks and maintain accurate contract records.
On-site
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Country Study Operations Manager to join our diverse and dynamic team. As a Country Study Operations Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards. Your role will involv…
Remote · Quebec, Quebec, Canada
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators.
Remote · Canada
Serve as the primary contact between investigational sites and the sponsor while conducting various site visits to ensure compliance with ICH-GCP and Health Canada regulations. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data quality and site documentation.
Hybrid · Brant County
You will oversee the contracts management process, negotiating agreements, and ensuring compliance with legal and regulatory requirements. Key responsibilities include managing the end-to-end contracts process and collaborating with internal departments to ensure alignment on contract terms.
Remote · Quebec, Quebec, Canada
You will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff to facilitate smooth study conduct.
On-site
Clinical Trial Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks. What You Will Do You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges. Ke…
Hybrid · Canada
The Clinical Trial Coordinator will manage trial and site administration, including tracking essential documents and updating clinical trial databases. They will also handle budgeting, agreements, and payments while supporting regulatory submissions and site start-up activities.
Hybrid · Kirkland
The Bilingual Clinical Trial Coordinator will manage trial and site administration, including tracking essential documents and updating clinical trial databases. They will also handle budgeting, agreements, and payments while supporting regulatory submissions and site start-up activities.
On-site · Canada
You will oversee contract management workstreams, ensuring deliverables meet quality and timeline expectations. Key responsibilities include developing the clinical budget and managing the end-to-end contracts process.
On-site · Canada
You will manage day-to-day clinical trial management activities, ensuring adherence to timelines, budget, and quality standards. Key responsibilities include collaborating with cross-functional teams and building strong relationships with trial investigators and stakeholders.
Remote · ["Montreal, Quebec, Canada"]
Clinical Research Associate - Montreal, Canada - Diabetes and Obesity ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You…
