iconplc - Remote work

Senior Clinical Research Associate sought in Frankfurt, Germany, to lead site monitoring, ensure ICH-GCP compliance, and drive data integrity for innovative trials. Requires 2+ years CRA experience, a scientific degree, and 60% travel. Join ICON’s dynamic team to advance therapies while enjoying ...

Senior Clinical Research Associate sought for a Warsaw-based role overseeing multi-site trial compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and expertise in GCP, data integrity, and site management. Responsibilities include monitoring sites, resolving issues, ...

Senior Clinical Research Associate (Ophthalmology) sought by ICON plc for West Coast (Portland, LA, Seattle). Leverage 5+ years of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and drive innovative trials. Enjoy competitive benefits including health insur...

Join ICON as a Clinical Research Associate (CRA II) in Santiago, Chile. Leverage 2+ years of experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy benefits like health insurance, retirement planning, and global employee support...

Senior Clinical Research Associate sought by ICON Plc in Frankfurt, Germany. Manage and monitor clinical trials, ensuring GCP and regulatory compliance across multiple sites. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from com...

Senior Clinical Research Associate sought by ICON Plc to lead vaccine studies in Frankfurt, Germany. This role demands 10+ months of CRA experience, fluency in German and English, and 60% travel for site monitoring. You will ensure GCP compliance, manage multiple sites, and drive data integrity. ...

Join a leading life sciences organization as a **Business System Adoption Specialist** in Blue Bell, PA. Leverage your 4+ years of experience in business analysis and change management to drive adoption of clinical trial systems like EDC. We seek a solution-oriented professional with strong prese...

Join ICON plc as an Evidence Delivery Specialist in Burlington, Canada. You will manage sponsor oversight, maintain inspection-readiness, and coordinate TMF/Master File QC. Ideal for candidates with a Bachelor's in life sciences, GCP/ICH knowledge, and strong collaboration skills. Enjoy benefits ...

Join ICON plc as an **Evidence Delivery Specialist** in Burlington, Canada. You will ensure inspection-readiness by managing TMF/Master File QC, customizing Expected Document Lists, and collaborating with CROs. Ideal for candidates with a Bachelor’s in life sciences, GCP/ICH knowledge, and strong...

ICON plc seeks a Study Manager in Warsaw, Poland, to drive clinical study delivery within a fully sponsor-dedicated program. Leveraging 3+ years of pharmaceutical experience and ICH-GCP expertise, you will manage end-to-end operations, budgets, and cross-functional teams. This role offers a chanc...

Seeking an experienced **eCOA Project Manager** to join ICON plc in Gdansk, Poland (also open to Bulgaria/South Africa). You will lead cross-functional eCOA projects, defining scope, managing budgets, and mitigating risks. Requires 3+ years of IRT/eCOA experience, strong leadership, and fluency i...