iconplc

ICON seeks a Clinical Trial Manager in Seoul, South Korea to drive clinical operations and deliver high-quality outcomes. You will manage study timelines, budgets, and compliance while collaborating with cross-functional teams and investigators. Requires a university degree, 3+ years of PMS/RMP C...

Senior Clinical Research Associate sought for a Frankfurt-based role. You will monitor trial sites, ensure GCP compliance, and manage multiple projects. Requires a Bachelor's in a scientific field, extensive CRA experience, and fluency in German and English. Benefit from competitive retirement pl...

Join ICON as a Clinical Research Associate and drive innovation in clinical trials. Leverage your 2+ years of CRA experience and ICH-GCP expertise to monitor sites, ensure data integrity, and advance therapies across the United States. Enjoy competitive benefits, health insurance, and retirement ...

ICON seeks a Director, Research Services, Oncology to lead clinical research in Blue Bell, PA. This role drives protocol development, study start-up, and regulatory submissions (FDA/EMA) for solid tumor programs. Requires 8+ years oncology experience, a life sciences degree (Pharm.D./Ph.D. prefer...

Lead clinical trial operations in Shanghai as a Manager at ICON plc. Oversee global study execution, ensuring regulatory compliance and on-time delivery. Requires a Bachelor's in science/healthcare, extensive clinical ops experience, and strong leadership skills. Enjoy benefits like health insura...

ICON seeks a Clinical Trial Manager in Milan, Italy, to drive clinical deliverables and ensure high-quality outcomes. You will manage trial operations, collaborate with cross-functional teams, and ensure regulatory compliance. Requires a university degree in medicine/science, subject matter exper...

Senior Clinical Trial Manager sought by ICON in Sydney, Australia. Leverage 10+ years of clinical trial management and CRO experience to oversee budgets, study start-up, and global trial integrity. Ideal for experts with monitoring and mentoring backgrounds seeking leadership in complex programs....

ICON plc seeks a Project Manager, IRT to lead Interactive Response Technology solutions for global clinical trials in Sofia, Bulgaria. You will manage IRT system implementation, cross-functional teams, and project timelines within a leading healthcare intelligence organization. Ideal candidates b...

Join ICON as a Site Contracts Negotiator II in Warsaw or Gdańsk. Independently manage and negotiate clinical trial agreements and budgets for diverse studies. Leverage your fluency in English and Polish, along with expertise in CRO or pharma contracting, to drive efficient study start-up. Enjoy c...

Join ICON plc as a Clinical Pricing & Payments Senior Associate in Barcelona, Spain. Leverage 3+ years of financial support experience to create clinical study budgets and pricing proposals. You will develop fair market value guidelines and maintain pricing tools in a home-based role. Enjoy compe...

Join ICON as a Site Specialist II in Warsaw, Poland. Manage site support activities, document collection, and study start-up for clinical trials. Requires fluency in English plus French, German, or Italian, a life sciences degree, and GCP knowledge. Enjoy benefits like annual leave, health insura...

ICON seeks a Clinical Research Associate I in Shanghai to design and monitor clinical trials, ensuring ICH-GCP compliance and data integrity. Ideal candidates hold a Bachelor's in science/healthcare with 1+ year CRA experience. This role involves site visits, protocol oversight, and collaboration...