iconplc

Join ICON plc as a Clinical Research Associate II in Buenos Aires. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive healt...

Join our dynamic team in Lenexa as a Lab Analyst I. Conduct routine tests to support vital clinical research studies. We seek a detail-oriented graduate in biology or chemistry, eager to develop laboratory skills. Enjoy competitive benefits including health insurance and a global support program.

Seeking a Senior Data Scientist specializing in Data Management for an office-based role in Blue Bell, PA or Raleigh, NC. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient linkage methodologies. This role offers competitive benefits and the chance t...

Join ICON plc, a global clinical research leader, in Salt Lake City. As a Medical Research Associate, you will conduct vital signs, phlebotomy, and participant screenings to support vital drug development. This role requires a clinical background and offers a competitive benefits package for your...

Join ICON plc's clinical research team in Houston as a Medical Research Associate. Support the design and execution of trials, ensuring data accuracy and quality. Requires a medical certification and strong organizational skills. Enjoy competitive benefits including health insurance and retiremen...

Join ICON plc as a Medical Research Associate (Phlebotomist/MA) in Houston, TX. This PRN, day-shift role is crucial for supporting clinical trials, ensuring precise data collection and compliance. Ideal candidates have medical certification, phlebotomy skills, and strong organizational abilities....

Join ICON plc as a Senior Statistical Programmer II in Montreal (remote). Utilize your advanced SAS and R-Shiny skills to analyze clinical trial data, ensuring statistical integrity. This role offers competitive benefits and a chance to shape the future of clinical development within a global lea...

Join ICON plc as a fully remote, client-dedicated Pharmacometrician. Utilize your Ph.D. and 3+ years of experience in model-based drug development, with expertise in NONMEM and Monolix. You will drive pharmacometric strategy for regulatory submissions and collaborate with multidisciplinary teams,...

Join our Portland team as a Senior Research Associate to develop and validate cutting-edge molecular assays for clinical trials. You will design studies, analyze data, and collaborate cross-functionally, leveraging 3+ years of lab experience and PCR expertise. We offer competitive benefits includ...

Join ICON plc, a global healthcare leader, as a Global Supply Chain Specialist in Dublin. You will optimize end-to-end supply chain processes, ensuring timely delivery and operational excellence. This role requires a degree and 2-4 years' experience in a global supply chain or procurement environ...

Join ICON plc as a Senior Clinical Data Coordinator in Mexico City. Utilize your 5-7 years of experience with RAVE or Veeva to ensure data quality and regulatory compliance. You will develop data management plans, mentor junior staff, and collaborate with cross-functional teams. We offer competit...

Lead regulatory submissions and strategy as a home-based Manager in Seoul. Utilize 6+ years of pharmaceutical regulatory experience to guide drug development from CTA to post-approval. Enjoy competitive benefits including health insurance and global support, driving excellence at a world-leading ...