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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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Site Management Associate I

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Join ICON plc, a global clinical research leader, as a Site Management Associate I in Kuala Lumpur. Support site monitoring and ensure protocol/GCP compliance in a dynamic team environment. A relevant degree and strong organizational skills are key. Enjoy competitive health insurance, retirement ...
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Malaysia , Kuala Lumpur
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Clinical Trial Assistant

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Join ICON plc, a global clinical research leader, as a Clinical Trial Assistant in Manila. Utilize your scientific background to coordinate trials, manage documentation, and ensure regulatory compliance. Enjoy competitive benefits while contributing to innovative healthcare advancements in a dyna...
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Philippines , Manila
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Regional Pharmacovigilance Senior Manager

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Lead regional pharmacovigilance activities for a global CRO. Oversee drug safety projects, ensure GVP compliance, and enhance safety processes. Requires 7-12 years' industry experience, including 5+ in PV. Offers competitive health insurance and retirement planning.
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Manager, Clinical Operations

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Lead clinical trial operations in Warsaw, ensuring efficiency and regulatory compliance. This pivotal role requires extensive experience in managing clinical operations and strong leadership skills. You will drive strategic planning, mentor teams, and contribute to innovative therapies. We offer ...
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Poland , Warsaw
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Global Clinical Delivery Manager

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Join ICON plc, a global healthcare intelligence leader, as a Global Clinical Delivery Manager in Sofia. Utilize your 5+ years of clinical research experience and project management skills to coordinate international trials from setup to archival. You will ensure study delivery to time, cost, and ...
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Bulgaria , Sofia
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Clinical Research Associate

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Join ICON plc, a global clinical research leader, as a CRA II/Senior CRA. Support high-impact trials for a large pharmaceutical company from Paris or Lyon. Requires 2+ years of monitoring experience, ICH-GCP knowledge, and fluency in French/English. Enjoy competitive benefits and shape the future...
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France , Paris; Lyon
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Senior Clinical Research Associate

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Greece , Athens
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Clinical Research Associate II

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Join ICON plc as a Clinical Research Associate II in Utrecht. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. Requires 2+ years CRA experience, fluency in Dutch/English, and 60% travel. We offer competitive health insurance and retirement plans.
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Netherlands , Utrecht
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Clinical Research Associate II

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Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Santiago, Chile. You will monitor sites, ensure protocol/GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% ...
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Chile , Santiago
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