ICON plc is a global leader in drug and device development, providing innovative consulting and commercialization services to enhance client outcomes and accelerate market entry.
Dublin
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Remote · Blue Bell, Pennsylvania, United States
The Principal Feasibility Analyst leads feasibility strategy and execution for clinical studies, synthesizing complex data to inform enrollment and site selection. They partner with cross-functional teams to provide strategic insights and mentor junior staff to ensure high-quality study planning.
Remote · Burlington, Prince Edward Island, Canada
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They are responsible for monitoring clinical sites, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
Remote · Montreal, Quebec, Canada, Toronto, Ontario, Canada
The Clinical Associate supports the planning, execution, and monitoring of clinical trials to ensure adherence to protocols and regulatory standards. They coordinate study activities, manage documentation, and collaborate with cross-functional teams to ensure successful trial delivery.
Remote · Montreal, Quebec, Canada
You will coordinate all activities for setting up and monitoring clinical studies while maintaining accurate documentation and study status reports. Additionally, you will manage sponsor queries, ensure cost efficiency, and foster collaborative relationships with clinical investigators and site staff.
Remote · Burlington, Prince Edward Island, Canada
The Study Start-up/Site Activation Lead manages country-level start-up activities, including regulatory documentation, site performance tracking, and submission of applications to authorities. They collaborate with local study teams to ensure milestones are met in compliance with ICH-GCP and client SOPs.
On-site · Burlington
Patient and Site Engagement Operations Specialist At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Patient and Site Engagement Operations Specialist at ICON, you will drive patient recruitment strategies for clinical trials. What You Will Do: You will manage day-to-day talent acquisit…
On-site · Burlington
Senior CRA / CRA II 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 govern…
On-site · Burlington
Clinical System Lead - United States, Canada, Mexico, Colombia (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 Senior Clinical System Lead to join ICON’s Full Service IOD Clinical Data Science team. The Senior Clinical System Lead will lead and direct one or more…
On-site · Burlington
Medical Monitor At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Medical Director at ICON, you will drive medical initiatives within project teams, guiding strategic direction and decision-making processes, and offer expert medical and scientific guidance, leveraging therapeutic experti…
On-site · Burlington
Senior Clinical Scientist - Oncology - Home Based (US) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. What you will be doing: May lead or support a study or studies, depending on size/complexity. If lead, accountable for the clinical/scientific execution of the protocol. As lead, will b…
On-site · Burlington
Trial Delivery Management (Advanced) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Trial Delivery Management (Advanced) at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives. What You Will Do: You will man…
On-site · Montréal
Clinical Research Associate - Quebec At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. We are looking for a C…
On-site · Burlington
Clinical Scientist - Infectious Disease (HIV) - Home Based (US/Canada) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. What you will be doing: May lead or support a study or studies, depending on size/complexity. If lead, accountable for the clinical/scientific execution of the protocol.…
On-site · Montréal
Senior CRA - Home-based (Canada) 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 devi…
Remote · Burlington, Prince Edward Island, Canada
The Site Engagement Lead will build and maintain strong relationships with clinical trial site staff to ensure study compliance and successful conduct. They will also monitor site performance metrics and implement engagement strategies to optimize site performance.
Remote · Blue Bell, Pennsylvania, United States
The Global Study Lead is responsible for managing project activities, including developing detailed project plans, budgets, and timelines to ensure successful delivery. They will lead cross-functional teams, monitor project progress, and engage with stakeholders to ensure alignment with organizational objectives.
Remote · Canada, Colombia, Mexico, United States
The Senior Clinical System Lead directs project teams in the initiation, planning, and maintenance of clinical data systems throughout the trial lifecycle. They also support business development efforts, perform quality control, and manage vendor interactions to ensure project timelines and budgets are met.
Remote · Burlington, Prince Edward Island, Canada
The Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are conducted, recorded, and reported in accordance with ICH-GCP and standard operating procedures.
Remote · Blue Bell, Pennsylvania, United States
You will lead and manage complex programs by coordinating cross-functional teams and ensuring deliverables meet quality, timeline, and budget expectations. Additionally, you will oversee site resourcing and workforce planning while implementing process improvements to enhance program efficiency.
Remote · Burlington, Prince Edward Island, Canada
Manage relationships with investigator sites to support clinical research performance and resolve operational issues. Collaborate with internal teams to align site capabilities with study requirements and drive quality improvements.
