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 · 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.
Remote · Montreal, Quebec, Canada, Quebec, Quebec, Canada
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. This includes conducting site visits, resolving issues, and collaborating with cross-functional teams to ensure accurate data collection.
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. Responsibilities include conducting site visits, resolving operational issues, and collaborating with cross-functional teams to ensure accurate data collection.
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.
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.
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 · 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 · 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.
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 align with SOPs, ICH-GCP, and applicable regulatory requirements.
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.