iconplc - Poland, Remote work

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 as a Clinical Research Associate II/Senior CRA in Warsaw or Poznan, Poland. Leverage your 1+ year of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy benefits like health insurance, retirement planning, and g...

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,...

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...

Join ICON plc as a Senior Clinical Research Associate in Warsaw. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, r...

Join ICON plc as a Clinical Research Associate II in Warsaw, Poland. Leverage your 1+ year of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and drive innovative clinical trials. Enjoy benefits like health insurance, retirement planning, and global employe...

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 in Warsaw as a Senior Clinical Research Associate. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your 3+ years of CRA experience and site management expertise in this travel-intensive role. We offer competitive health ins...

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...