iconplc - IT - Administration

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...

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...

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 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...

Senior Clinical Research Associate sought by ICON Plc to oversee clinical trials in Warsaw or Gdansk, Poland. This role demands a Bachelor's in a scientific field, extensive CRA experience, and expertise in site management, GCP, and regulatory compliance. You will monitor sites, ensure data integ...

Senior CRA opportunity at ICON plc, a world-leading clinical research organization. Based in Warsaw or Gdansk, Poland, this role involves overseeing clinical trials, ensuring GCP and regulatory compliance, and managing multiple sites. Requires a Bachelor's in a scientific field, extensive CRA exp...

Seeking an experienced **CRA II** in **Hangzhou, China** to conduct site monitoring and ensure ICH-GCP compliance. Requires a Bachelor's in science/healthcare and 2+ years of clinical research experience. Enjoy competitive benefits including health insurance, retirement planning, and flexible per...

Join ICON plc as a CRA II or Senior CRA in a home-based role across the U.S. (Portland, Salt Lake City, Houston, Downers Grove, Lawrence). You will independently monitor clinical trials, ensure ICH-GCP compliance, and safeguard data integrity. Requires a Bachelor’s degree, 1-3+ years of monitorin...

Senior Manager, Regulatory Strategy role in Raleigh, US. Leverage 7+ years of regulatory expertise to design clinical trials, develop submission plans, and advise ICON clients. Requires a Bachelor's in science/healthcare, supervisory experience, and strong strategic drug development skills. Benef...