iconplc - Poland, Warsaw

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 plc as a Clinical Data Coordinator I in Warsaw, Poland (hybrid). You will design and analyze clinical trials, manage eCRF development, and review complex medical data. Ideal for candidates with a Master’s in Life Sciences and basic clinical data management knowledge. Enjoy competitive b...

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 plc as a Clinical Pricing & Payments Senior Associate in Barcelona, Spain. Leverage 3+ years of financial support experience to create clinical study budgets and pricing proposals. You will develop fair market value guidelines and maintain pricing tools in a home-based role. Enjoy compe...

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...

Join ICON as a Graduate Pharmacovigilance Associate in Warsaw, Poland. Support global drug safety by collecting and processing adverse event data, preparing regulatory reports, and collaborating with cross-functional teams. Ideal for life science or pharmacy graduates with strong attention to det...

ICON plc seeks a Medical Data Reviewer in Warsaw, Poland. Leverage your Registered Nurse or life sciences background to ensure clinical data plausibility and consistency. You will independently draft Medical Data Review Plans and coordinate with Biometrics teams. Enjoy competitive benefits includ...