iconplc - On-site work

Join ICON plc in Mexico City as a Clinical Trial Associate. You will coordinate clinical trials, manage documentation, and ensure protocol compliance. We seek a detail-oriented graduate with clinical research knowledge and strong organizational skills. Enjoy competitive benefits including health ...

Join ICON plc as a Clinical Site Associate in Paris. Support clinical trial operations, ensure site compliance, and prepare for audits while building skills towards a CRA role. Requires a life sciences degree, fluency in French/English, and offers comprehensive benefits. This office-based positio...

Join ICON plc as a Clinical Site Associate in Bucharest, Romania. You will support clinical trial operations, ensuring site compliance and documentation accuracy. This office-based role with flexibility is a direct pathway to a traveling CRA position. Requires a life sciences degree, strong organ...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Shanghai. Utilize your life sciences degree and clinical research experience to support trial design, implementation, and monitoring. You will ensure protocol adherence and data integrity while collaborating with c...

Join Accellacare, part of ICON's network, as a Sr Clinical Research Nurse in Hickory, US. Autonomously coordinate and conduct clinical trial procedures, ensuring protocol compliance and patient care. Requires an RN/LPN license and strong GCP knowledge. Enjoy competitive benefits including health ...

Lead bioanalytical laboratory operations at ICON in Whitesboro, NY. Oversee a team, manage workflows, and ensure GLP compliance to deliver high-quality data for clinical trials. Requires a relevant degree, lab management experience, and strong leadership skills. We offer competitive health insura...

Join ICON plc as a Scientist I in Whitesboro, NY. You will develop and perform assays for clinical trials, ensuring compliance with GLP/GCP standards. The role requires a Bachelor's in Biology or related field and experience with binding assays. We offer a competitive salary, annual bonus, and co...

Join ICON in Shanghai as a Site Specialist II, a key role in clinical trial execution. You will conduct site visits, ensure protocol/GCP compliance, and manage data integrity. Requires a Bachelor's degree, 3+ years of SSU experience, and strong organizational skills. We offer competitive benefits...

Join ICON plc, a global clinical research leader, as a Clinical System Designer I in Bangalore. You will design and implement clinical data management systems (CDMS) and eCRFs, ensuring they meet trial protocols and regulatory standards. This role requires functional knowledge of CDMS tools and t...

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.

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...