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.
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.
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
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 · ["Burlington, Prince Edward Island, Canada"]
Clinical Trial Associate 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 Trial Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. What You Will Do: You will lead on clinical coordination tasks requi…
Remote · ["Burlington, Prince Edward Island, Canada", "Vancouver, British Columbia, Canada"]
Clinical Research Associate 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 analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is a sponsor dedicated position focused on monitoring obes…
On-site · Canada
The Clinical Research Associate will monitor clinical trial sites to ensure adherence to protocols and regulatory requirements. They will conduct site visits, collaborate with teams, and provide training to maintain high standards of clinical trial conduct.
Remote · ["Blue Bell, Pennsylvania, United States"]
DCT Lead 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 Clinical System Lead, working as a Decentralized Clinical Trials Lead exclusively assigned and embedded within a Pharmaceutical Company, you will provide strategic leadership and direction in the design, development, and implementation of eCO…
Remote · ["Montr\u00e9al, Quebec, Canada"]
Senior CRA 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. Overview: ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and pub…
Remote · ["Burlington, Ontario, Canada"]
Clinical Trial Transparency Specialist 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 Clinical Trial Transparency Associate at ICON, you will be responsible for processing the anonymization of clinical trial documents and datasets required for public disclosure. The Anonymization Specialist will partner with internal and external collaborators on the planning, initiation, and del…