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Sr Clinical Research Nurse

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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 ...
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Location
United States , Hickory
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Not provided
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Manager, Bioanalytical Services

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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...
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Location
United States , Whitesboro
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Salary
100472.00 - 125590.00 USD / Year
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Scientist I

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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...
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Location
United States , Whitesboro
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Salary
46864.00 - 58580.00 USD / Year
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Site Specialist II

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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...
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China , Shanghai
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Clinical System Designer

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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...
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India , Bangalore
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Not provided
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Lab Analyst I

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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.
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Location
United States , Lenexa
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Medical Research Associate

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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...
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United States , Salt Lake City
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Medical Research Associate

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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...
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United States , Houston
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Medical Research Associate

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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....
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United States , Houston
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Senior Research Associate

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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...
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Location
United States , Portland
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Global Supply Chain Specialist

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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...
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Location
Ireland , Dublin
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Clinical Trial Administrator

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Join ICON plc as a Clinical Trial Administrator in Mexico City. Support the design and analysis of clinical trials, ensuring protocol compliance and managing essential documentation. This role requires a scientific degree, knowledge of trial processes, and strong organizational skills. We offer c...
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Location
Mexico , Mexico City
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