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.
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.
Hybrid · Burlington
The Clinical Trial Associate will assist in the coordination and administration of clinical trials while ensuring compliance with regulatory protocols. They will also maintain essential study documentation and facilitate communication across cross-functional teams to ensure smooth trial execution.
Remote · Burlington, Prince Edward Island, Canada
You will oversee and support the execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and project timelines. This involves managing site activities, collaborating with cross-functional teams, and implementing strategies to mitigate clinical trial risks.
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.
Remote · Canada, Colombia, Mexico
The Principal Clinical Data Science Programmer will lead the programming of clinical data management systems, including eCRF and edit checks, and develop analytics solutions for clinical trials. They will also collaborate with cross-functional teams to ensure data integrity and provide technical leadership for automation and process improvement initiatives.
Remote · Canada
Develop, validate, and maintain programming solutions for clinical data management systems and data validation outputs. Collaborate with cross-functional teams to ensure the integration of programming solutions into the clinical trial data management process.
Remote · Canada, Colombia, Mexico, United States
The Clinical System Lead directs project teams in the initiation, planning, maintenance, and closing of clinical trial systems. They also support business development, manage vendor interactions, and ensure quality control of technical documentation.
Remote · Canada
The Payment Specialist is responsible for executing site and participant payments in compliance with clinical trial agreements and regulatory requirements. They also coordinate with internal teams and stakeholders to resolve payment issues and ensure high-quality financial execution.
Remote · Canada, Colombia, Mexico
The Clinical System Designer I leads the design and development of clinical systems, ensuring alignment with study protocols and operational requirements. They are responsible for creating custom CRF screens, managing edit check specifications, and overseeing post-production database changes.
Remote · Canada
The Senior Clinical System Designer leads the design and development of clinical systems, ensuring alignment with study protocols and operational requirements. They are responsible for creating custom CRF screens, managing edit check specifications, and driving post-production database changes.
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.
Remote · Montreal, Quebec, Canada
The Senior 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 accurately conducted, documented, and reported according to ICH-GCP standards.
Remote · Mexico
The Operations Manager will oversee the execution of clinical trials, ensuring adherence to protocols, timelines, and regulatory standards. They are responsible for coordinating clinical operations delivery, mentoring junior staff, and engaging with cross-functional teams to optimize trial design.
Remote · Burlington, Prince Edward Island, Canada
The Site Partner II is responsible for coordinating site activation and maintenance activities across multiple studies to ensure timely project delivery. They act as the primary liaison for sites, managing documentation, mitigating risks, and ensuring compliance with regulatory standards and ICON SOPs.
Remote · Vancouver, British Columbia, Canada
Serve as the primary contact between investigational sites and sponsors while conducting all types of site visits. Ensure site compliance with ICH-GCP and Health Canada regulations while managing data quality and patient safety reporting.
Remote · Burlington, Prince Edward Island, Canada
Oversee and coordinate the end-to-end preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies. Serve as a primary escalation point for contract issues while collaborating with legal, finance, and project teams to ensure alignment.
Hybrid · Burlington
The Workday Integration Manager will oversee the strategy, implementation, and optimization of HR technology solutions while providing leadership to the functional HRIS team. They are responsible for managing Workday operations, governance, supplier contracts, and ensuring alignment with global design standards.
Remote · Burlington, Prince Edward Island, Canada
The Senior Clinical Research Associate is responsible for independently setting up and monitoring clinical studies while ensuring adherence to ICH-GCP regulations. They will also manage regulatory submissions, handle sponsor queries, and contribute to study documentation and site management.
Remote · Canada
The Director will lead regulatory strategy for drugs, biologics, and combination products while acting as a subject matter expert for the Canadian market. They are responsible for managing client interactions, overseeing regulatory submissions to Health Canada, and coaching team members to ensure project success.
Hybrid · Montréal
Lead the global function responsible for planning, forecasting, and deploying clinical delivery talent across a large portfolio. Balance resource demand and capacity while challenging business partners to ensure delivery quality and margin protection.
