iconplc - Poland, IT - Administration

Join ICON as a Clinical Trial Associate in Warsaw, Poland. Support innovative clinical research by coordinating trials, managing documentation, and ensuring regulatory compliance. Ideal for candidates with a scientific degree and knowledge of clinical processes. Enjoy benefits like health insuran...

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....

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...

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...

Join ICON as a Study Support Assistant in Warsaw, Poland, and play a key role in advancing clinical trials. We seek candidates with a high school diploma (Bachelor’s preferred) and administrative experience, ideally in healthcare. You will manage study documents, coordinate meetings, and ensure r...

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 ...