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.
Hybrid · Burlington
The role involves coordinating and administering clinical trials while ensuring compliance with protocols and regulatory requirements. You will also maintain essential study documentation and collaborate with cross-functional teams to facilitate smooth trial execution.
Hybrid · Toronto
The associate will assist in the coordination and administration of clinical trials while ensuring compliance with protocols and regulatory requirements. They will also maintain essential study documentation and collaborate with cross-functional teams to facilitate smooth trial execution.
Remote · Canada
The specialist will manage and execute site and participant payments in compliance with clinical trial agreements and regulatory requirements. They will also act as a subject matter expert, coordinating with internal teams and stakeholders to resolve payment issues and optimize financial processes.
On-site · Canada
Manage and execute site and participant payments in compliance with clinical trial agreements and regulatory requirements. Coordinate with cross-functional teams to resolve payment issues and optimize payment processes.
On-site · Montréal
Accountable for the performance, compliance, and financial oversight of assigned clinical trial protocols within a specific country. Responsibilities include managing country budgets, executing regulatory submissions, and coordinating with internal and external stakeholders to ensure site readiness.
Remote · Canada
The role involves leading site management activities, mentoring junior team members, and developing site start-up documentation. The CRA will also manage study sites remotely and face-to-face while ensuring adherence to monitoring guidelines and KPIs.
Hybrid · Kirkland
Manage clinical trial administration, including document tracking, eTMF reconciliation, and regulatory submissions for site start-up. Coordinate site budgets, contract negotiations, and payment execution while ensuring compliance with local legislation and guidelines.
Remote · Canada, United States
Lead the operational execution of global clinical trials, managing the Clinical Trial Team, vendors, and budgets to ensure deliverables are met. Oversee trial set-up, recruitment planning, risk assessment, and inspection readiness for infectious disease and vaccine studies.
Remote · Canada, United States
Provide operational leadership across the full clinical study lifecycle, overseeing study management, site management, and vendor activities. Lead global clinical trials from sourcing and start-up through execution and database release to ensure high-quality data delivery.
On-site · Canada
Oversee the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies. Coordinate contract management workstreams and serve as the primary escalation point for contract issues.
On-site · Toronto
The role involves identifying, initiating, and closing out investigational sites for phase II-IV clinical studies while ensuring adherence to ICH-GCP regulations. Responsibilities include monitoring studies, preparing regulatory submissions, and managing study cost efficiency.
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…
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…
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.
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…
Remote · ["Canada", "Colombia", "Mexico"]
Clinical System Lead - Canada, Colombia, Mexico (Remote) 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. We have an incredible opportunity for a Clinical System Lead to join ICON’s Full-Service IOD Clinical Data Science team. The Clinical System Lead (CSL) will lead and direct one or more Clinical Data Science (C…
Remote · ["Blue Bell, Pennsylvania, United States"]
Senor 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 Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. What You Will Do: You will oversee medi…
Remote · ["Blue Bell, Pennsylvania, United States"]
Clinical Budget Analyst - Senior 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 Clinical Budget Analyst - Senior at ICON, you will be essential in developing and analyze pricing strategies for clinical trial investigators. What You Will Do: You will lead on pricing and investigator payments tasks requiring…
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. As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. What You Will Do You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations. Key…
