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 · 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.
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.
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.
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.
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.
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.
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.
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.
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 · 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 · 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.