iconplc - Poland, IT - Administration, Remote work

Join ICON as a Clinical Research Associate (CRA II) in Warsaw, Poland. Leverage 2+ years of experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy benefits like health insurance, retirement planning, and global employee support....

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...

Senior CRA role in Warsaw, Poland. Seeking a Clinical Research Associate with 2+ years of experience, a scientific degree, and ICH-GCP expertise. Responsibilities include site monitoring, data integrity, and protocol compliance. Benefits include health insurance, retirement planning, and global e...

ICON plc seeks a Clinical Supplies Project Manager to join its world-leading clinical research team in Warsaw or Gdansk, Poland. You will manage global supply planning, forecasting, and IRT system setup for clinical trials. Ideal candidates bring 4+ years of clinical supply experience, strong pro...

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 ...

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,...

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 ...