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
You will manage contract activities including negotiating clinical trial agreements, budgets, and payment terms with assigned sites. Additionally, you will partner with internal teams to improve site activation metrics and ensure project standards are met.
Remote · Burlington, Prince Edward Island, Canada
You will lead and manage complex programs by overseeing site resourcing, workforce planning, and cross-functional team coordination. Additionally, you will be responsible for developing program plans, managing budgets, and identifying process improvements to enhance efficiency.
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
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
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, 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 · Cary, North Carolina, United States
The Senior Medical Writer will lead the preparation, review, and editing of complex clinical study documents and regulatory submissions. They will also collaborate with cross-functional teams to interpret clinical data and mentor junior staff to foster a culture of excellence.
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 · Canada, United States
The Project Manager oversees clinical research projects or portfolios, serving as the primary client liaison to ensure deliverables are met on time and within budget. They lead cross-functional teams, manage project financials, and participate in bid defense processes while maintaining high quality standards.
Remote · Canada
The Site Activation Partner facilitates the initiation of clinical trials by preparing regulatory documents and coordinating with stakeholders to obtain necessary approvals. They also support study teams in developing essential study documents and ensure compliance with regulatory requirements throughout the start-up process.
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.
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, 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.
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 · 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.
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.
