iconplc - United States

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 clinical research leader, as a Research Operations Coordinator in the United States. Support project execution and clinical trial coordination within the pharmaceutical industry. Utilize your organizational skills and life sciences background in a dynamic team. Enjoy compe...

Seeking a Global Study Manager with 3+ years in clinical trial management, including phase I oncology. You will oversee global study execution, vendor management, and key document development. This remote US role (Eastern/Central time) offers competitive health insurance and retirement benefits a...

Lead strategic procurement for clinical trials as a Senior Manager at ICON. Utilize your IVRS expertise and healthcare sourcing background to drive cost efficiencies and supplier relationships. This US-based role offers competitive benefits, focusing on data-driven decisions and cross-functional ...

Join ICON plc, a global clinical research leader, as a Medical Research Associate in San Antonio. This role is ideal for an ACLS-certified Paramedic/EMT to conduct vitals checks, phlebotomy, and screen participants. We offer competitive pay, comprehensive health insurance, and a flexible benefits...

Join ICON plc, a global clinical research leader, as a Set Up Specialist. You will coordinate clinical trial setup, ensuring regulatory compliance and efficient study execution. This role requires a life sciences degree and experience in trial setup or site management. The position offers competi...

Join our winning lab team at ICON plc, a top-rated employer. We seek a Scientist II in Whitesboro, NY to develop and perform GLP/GCP assays for clinical trials. The role requires a Bachelor's in Biology/Chemistry and experience with binding assays. We offer a competitive salary, bonus, and compre...

Join ICON plc as a Senior Clinical Research Associate (CRA) and shape the future of clinical development. Oversee trial activities, ensure protocol/GCP compliance, and manage site performance across multiple projects. This role requires extensive CRA experience, strong monitoring skills, and 60% ...

Join ICON in San Antonio as a CMC Project Manager I. You will lead CMC projects for early-phase drug development, ensuring GMP compliance and coordinating cross-functional teams. This role requires 1+ years of project management experience in a pharmaceutical setting. We offer competitive health ...

Join ICON plc, a global clinical research leader, as a Project Manager I EDS. This hybrid role in Whitesboro, NY requires 3+ years of lab or project management experience. You will manage bioanalytical project timelines, budgets, and client coordination. We offer competitive health insurance, ret...

Lead US clinical trials as a Local Study Associate Director at ICON plc. This role requires 5+ years of US trial management experience and deep ICH-GCP knowledge. You will oversee study commitments, lead local teams, and ensure regulatory compliance. We offer competitive health insurance, retirem...

Join ICON plc, a global clinical research leader, as a Clinical Study Coordinator in Salt Lake City. You will design trials, analyze medical data, and advance innovative therapies. The role requires a scientific degree, GCP knowledge, and strong organizational skills. We offer competitive benefit...