iconplc

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...

ICON plc seeks a Project Manager to lead clinical research projects, ensuring on-time, on-budget delivery with top quality. You will manage cross-functional teams, stakeholder communication, and risk mitigation. Ideal candidates have a Bachelor's degree, proven project management experience, and ...

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...

Senior Site Contracts Negotiator sought to lead complex clinical trial agreement and budget negotiations across multiple countries. Join ICON’s dynamic team in Sofia, Warsaw, or Bucharest. Requires a Bachelor’s degree and significant CRO/pharma contracting experience. Enjoy competitive benefits i...

Senior Clinical Research Associate – home-based across Canada. Join ICON, a world-leading clinical research organization, to monitor trial progress ensuring ICH-GCP and regulatory compliance. Ideal for candidates with a scientific degree, 1-3+ years of monitoring experience, and 70% travel flexib...

Entry-level Clinical Research Associate role in São Paulo, Brazil. Requires a Bachelor’s in science/healthcare and 2+ years of CRA experience. You will conduct site visits, ensure ICH-GCP compliance, and manage data integrity. Benefits include health insurance, retirement plans, and global employ...

Join ICON plc as a Senior CRA in Montreal, Canada. Leverage your 3+ years of clinical monitoring experience (oncology preferred) to ensure trial compliance with ICH-GCP and regulations. This role requires 70% travel and offers comprehensive benefits, including health insurance, retirement plannin...

Senior Clinical Research Associate sought by ICON Plc to oversee clinical trials in Blue Bell or Durham, US. Requires a Bachelor’s in a scientific field, extensive CRA experience, and ophthalmology expertise. Manage multiple sites, ensure GCP compliance, and drive data integrity with 60% travel. ...

Senior Clinical Research Associate (CRA) needed in Dallas or Houston, TX. Leverage your ophthalmology expertise to oversee multi-site trials, ensuring GCP and regulatory compliance. This role demands strong site management, data integrity, and travel (60%). Join ICON Plc for competitive benefits,...