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ICON plc

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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

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Biotechnology Research
5,001+ people

About

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.

Open positions

Senior Clinical Research Associate

On-site · Burlington

Senior Clinical Research Associate, Eastern 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. 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. This is…

Senior Clinical Research Associate

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…

Clinical Research Associate

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…

Senior Clinical Research Associate

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…

Senior Clinical Research Associate

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.

Senior Clinical Research Associate

Remote · Canada

Monitor the progress of clinical studies at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. Maintain accurate records and reports in accordance with ICH-GCP and standard operating procedures.

Senior Clinical Trial Manager

Remote · United States

Lead the operational delivery of clinical trials from study start-up through closeout while ensuring quality and compliance. Manage cross-functional stakeholders, study timelines, budgets, and site performance to drive successful trial outcomes.

Clinical Research Associate

Remote · Burlington, Prince Edward Island, Canada

The Clinical Research Associate will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving operational issues, and collaborating with cross-functional teams to ensure accurate data collection.

Senior Clinical Research Associate

Remote · Burlington, Prince Edward Island, Canada

The Senior Clinical Research Associate will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and industry standards. Responsibilities include monitoring clinical sites, resolving operational issues, and collaborating with cross-functional teams to ensure accurate data collection.

Clinical Research Associate

Remote · Burlington, Prince Edward Island, Canada, Toronto, Ontario, Canada

You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving operational issues, and collaborating with cross-functional teams to ensure accurate data collection.

Clinical Research Associate

Remote · Burlington, Prince Edward Island, Canada

You will conduct clinical trial monitoring activities including site visits, protocol compliance, and data integrity maintenance. Additionally, you will collaborate with investigators and site staff to ensure the smooth conduct of clinical trials and the preparation of study documentation.

Clinical Research Associate

Remote · Burlington, Prince Edward Island, Canada

The Clinical Research Associate will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving operational issues, and collaborating with cross-functional teams to ensure accurate data collection and reporting.

Clinical Trial Associate

Hybrid · Burlington

Coordinate and administer clinical trials, maintain study and regulatory documentation, and support the preparation of study materials. Collaborate with cross-functional teams and track and report trial metrics and milestones to support smooth trial execution.

Senior Clinical Trial Associate

Remote · Burlington, Prince Edward Island, Canada

The Senior Clinical Trial Associate will oversee and coordinate clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines. They will collaborate with cross-functional teams to manage site operations, ensure data integrity, and implement strategies to mitigate trial risks.

Clinical Trial Coordinator - Regulatory/Finance - Montreal, Canada

Hybrid · Montréal

Manage clinical trial administration, including document tracking, eTMF reconciliation, and regulatory submissions. Handle financial duties such as developing site budgets, negotiating contracts, and executing payments to investigators and vendors.

Clinical Trial Manager

Hybrid · Montréal

The Clinical Trial Manager is responsible for the performance, compliance, and financial oversight of assigned clinical protocols within a country. They manage site budgets, regulatory submissions, and coordinate with internal and external stakeholders to ensure trial milestones are met.

Senior Clinical Research Associate

Remote · Montreal, Quebec, Canada

Monitor the progress of clinical studies at investigative sites or remotely to ensure trials are conducted according to protocol. Ensure all recording and reporting comply with SOPs, ICH-GCP, and applicable regulatory requirements.

Clinical Research Associate

Remote · Canada

Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Monitor trial sites, conduct performance assessments, and collaborate with cross-functional teams to ensure data integrity and participant safety.