iconplc - Poland

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...

Global Data Manager sought in Warsaw, Poland, to lead clinical data analysis and strategy for ICON. This role requires a Bachelor's degree in life sciences or computer science, extensive clinical data management experience, and strong leadership skills. You will oversee data governance, integrate...

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...

Senior CRA, home-based in Poland. Join ICON, a world-leading clinical research organization, to oversee trial activities ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from flexible work, he...

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 ...