iconplc - Hybrid work

Join ICON plc in Mexico City as a Clinical Trial Associate and drive innovation in clinical research. Support trial coordination, regulatory compliance, and documentation while collaborating with cross-functional teams. Ideal for candidates with a scientific degree and knowledge of clinical trial...

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 Plc as a Clinical Trial Associate in Seoul, South Korea. Support clinical trial execution with 1+ year SC/CRC experience; IIT/SIT CRA experience preferred. This hybrid role (60% office-based in YeoEuiDo, 40% home-based) involves managing access programs, essential documents, budgets, an...

Senior Regulatory Affairs Specialist sought by ICON plc in Seoul, South Korea. Leverage 3+ years of pharmaceutical or medical device experience to ensure compliance and drive successful product registration. This role demands expertise in drug development, national regulations, and strategic regu...

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...

Senior or Lead Clinical Research Associate sought in Taipei, Taiwan. Join ICON to design and monitor global trials, ensuring ICH-GCP compliance and data integrity. Requires 2+ years CRA experience, a scientific degree, and 60% travel. Oncology experience valued. Benefits include health insurance,...

ICON seeks a Clinical Trial Manager in Milan, Italy, to drive clinical deliverables and ensure high-quality outcomes. You will manage trial operations, collaborate with cross-functional teams, and ensure regulatory compliance. Requires a university degree in medicine/science, subject matter exper...

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 in Sydney as a Clinical Site Associate / Clinical Trial Associate. Support site activation, essential document management, and CRA coordination in a hybrid office-based role. Ideal for candidates with a life sciences degree and initial clinical research experience. Enjoy benefits li...

ICON plc seeks a strategic Talent Acquisition Business Partner in Raleigh or Blue Bell, PA. You will drive full-cycle recruitment for healthcare and clinical research roles, leveraging data insights and ATS proficiency. This role demands strong stakeholder collaboration and a commitment to DEI. E...