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Site Management Associate II

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Join ICON as a Site Management Associate II in Buenos Aires, Argentina. Leverage 3+ years of clinical trial administration experience to lead TMF and eISF oversight, mentor new CTAs, and ensure GCP compliance. This role offers leadership development, health insurance, and retirement planning. Adv...
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Argentina , Buenos Aires
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Not provided
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Clinical Study Specialist

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United States , Basking Ridge
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Clinical Study Specialist

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Clinical Study Specialist role at ICON plc, a global leader in clinical research. Based in Warren NJ, Armonk NY, or Cambridge MA (hybrid). Requires a Bachelor’s degree and 2+ years industry experience supporting global trials with TMF, CTMS, and SharePoint. Enjoy competitive benefits, annual leav...
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United States , Boston; Basking Ridge, NJ
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Study Start-up Manager-South Korea-ICON Strategic Solutions

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South Korea , Seoul
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Senior Clinical Research Associate

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Senior Clinical Research Associate (CRA II) sought for a hybrid role in Bucharest, Romania, specializing in oncology. You will independently monitor clinical trials, ensuring GCP and regulatory compliance across SSVs, SIVs, IMVs, and COVs. Requires 18+ months of on-site monitoring experience, a l...
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Romania , Bucharest
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Clinical Research Associate II

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Join ICON as a Clinical Research Associate II in Seoul, South Korea. Leverage 2+ years of CRA experience and ICH-GCP expertise to design and monitor clinical trials, ensuring data integrity and patient safety. Enjoy extensive travel (60%), competitive benefits, and global support. Advance innovat...
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South Korea , Seoul
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Clinical Site Associate

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Join ICON plc as a Clinical Site Associate in Tel Aviv. Support site management for clinical trials, ensuring efficiency and compliance. A life sciences degree and strong organizational skills are key. Enjoy a hybrid role with competitive health insurance and retirement benefits.
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Location
Israel , Tel Aviv
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Clinical Trial Assistant

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Join ICON plc as a Clinical Trial Assistant (CTA) in a hybrid role based in Sofia, Bulgaria. You will support clinical trial design, analysis, and document management using systems like eTMF. This role requires a scientific degree, trial process knowledge, and strong organizational skills. We off...
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Bulgaria , Sofia
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Clinical Site Associate

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United Kingdom , Reading
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Clinical Study Specialist

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United States , Warren, NJ or Cambridge, MA
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Business Operations Analyst

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United States , Cambridge; Philadelphia
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Senior Clinical Research Associate

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Join ICON plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in German and English, and 60% travel. Enjoy competitive benefits including health insurance and...
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Germany , Frankfurt
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