iconplc - Poland, IT - Administration

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...

Join ICON plc as a Site Management Associate II with French in Warsaw. Support clinical trial site management, ensuring GCP compliance and protocol adherence. Requires a Bachelor’s in life sciences, clinical research experience, and fluency in English and French. Enjoy benefits like annual leave,...

Seeking a detail-oriented Clinical Research Coordinator for an office-based role in Gliwice/Bytom. You will support oncology studies, ensuring protocol and ICH-GCP compliance while managing site activities and data entry. This role requires fluency in English and Polish, along with proven oncolog...

Join ICON plc as a TMF Lead in Warsaw. Oversee Trial Master File management, ensuring regulatory compliance and integrity in clinical trials. Utilize your expertise in TMF processes within a world-leading clinical research organization. Enjoy competitive benefits including health insurance and re...

Lead clinical trial operations in Warsaw, ensuring efficiency and regulatory compliance. This pivotal role requires extensive experience in managing clinical operations and strong leadership skills. You will drive strategic planning, mentor teams, and contribute to innovative therapies. We offer ...

Join ICON plc as a Senior Clinical Associate in Warsaw. Support clinical trial management with a focus on inspection readiness and document management. Requires a Bachelor's degree and 2+ years of CTA experience in Pharma/CRO. We offer competitive benefits including health insurance and retiremen...

Join ICON plc, a global leader in clinical research, as a Clinical Site Associate in Warsaw. This hybrid role is key to ensuring site compliance and documentation accuracy for clinical trials. We seek a detail-oriented professional with a life sciences degree and strong organizational skills. Enj...

Join ICON plc as a Clinical Research Coordinator in Łódź. You will support clinical project execution, analyze data, and ensure operational success. We require a relevant degree, project experience, and strong analytical skills. Enjoy competitive benefits including health insurance and a global s...

Join ICON plc, a global clinical research leader, as a Contract Analyst I in Warsaw. Utilize your 5+ years of CRO/pharma contract negotiation experience to prepare and finalize clinical trial agreements and budgets. This role offers competitive benefits, including health insurance and retirement ...