iconplc - Poland, Remote work

ICON seeks a Clinical Project Manager for Post Trial Access in Gdansk, Poland. You will lead global PTA programs for investigational products, managing timelines, budgets, and cross-functional teams. Requires 2+ years in clinical research or biopharma, with expertise in regulatory frameworks and ...

Join ICON as a Payment Specialist in Warsaw, Poland. You will manage investigator payments for clinical trials, ensuring compliance with regulations like the Sunshine Act. Ideal candidates have a Bachelor’s in Finance and 1-2 years of experience in accounting or pharmaceutical finance. Enjoy bene...

Senior Clinical Research Associate sought by ICON plc, a world-leading clinical research organization, to oversee trial activities in Warsaw or Gdansk, Poland. You will ensure protocol compliance, data integrity, and participant safety while managing multiple sites. Requires extensive CRA experie...

Senior Clinical Research Associate sought for a Warsaw-based role overseeing multi-site trial compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and expertise in GCP, data integrity, and site management. Responsibilities include monitoring sites, resolving issues, ...

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...

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...

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...