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Clinical Research Associate

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Join ICON Plc in Shanghai as a Clinical Research Associate. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel. Enjoy health insurance, competitive retirement plans, and a global s...
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Location
China , Shanghai
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Not provided
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Clinical Site Manager II

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Join ICON Plc as a Senior Clinical Research Associate (CRA) in Paris. Oversee clinical trial sites, ensuring protocol adherence, GCP compliance, and data integrity. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, r...
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Location
France , Paris
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Not provided
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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 trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive monitoring and site management expertise in a role requiring ~60% travel. Enjoy competitive benefits inclu...
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Location
Germany , Frankfurt
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Clinical Research Associate II

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Join ICON plc as a Clinical Research Associate II in Beijing. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This office-based role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirem...
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Location
China , Beijing
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Senior Clinical Research Associate

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Join ICON Plc as a Senior Clinical Research Associate in Milan. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. Enjoy health insurance, competitive retirement plans, and glo...
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Location
Italy , Milan
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Not provided
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Clinical Research Associate

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Join ICON plc in Shanghai as a Clinical Research Associate. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement planning, an...
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Location
China , Shanghai
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Not provided
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Senior Clinical Research Associate

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Join ICON plc, a global leader in clinical research, as a Senior CRA or CRA II. You will design and analyze trials, ensure protocol compliance, and advance innovative therapies. The role requires 1-3+ years of monitoring experience, ICH-GCP knowledge, and 60% travel. We offer competitive health i...
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Location
United States , LOS ANGELES, PORTLAND, SAN ANTONIO, BLUE BELL, LONG BEACH
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Clinical Research Associate II

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Join ICON plc as a Clinical Research Associate II in Taipei. You will design trials, analyze medical data, and advance new therapies. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer health insurance, competitive retirement plans, and flexible work arrange...
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Taiwan , Taipei
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Intern

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Join ICON plc, a global healthcare intelligence leader, for a hands-on Summer Internship in Whitesboro, NY. Gain practical experience supporting clinical research projects while developing key professional skills. This full-time, onsite role is ideal for a current Bachelor's or Master's student s...
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Location
United States , Whitesboro
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Summer intern

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Join ICON plc, a global clinical research leader, for a hands-on Summer Internship in Whitesboro, NY. Gain practical experience supporting key projects while developing skills in research, analysis, and operations. This onsite role is ideal for a current Bachelor's or Master's student seeking to ...
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Location
United States , Whitesboro
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Global Study Manager

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Join ICON plc as a Global Study Manager in Reading, UK. Lead the design and analysis of global clinical trials, ensuring regulatory compliance. Utilize your 5+ years of trial management expertise to advance innovative therapies. We offer competitive benefits including health insurance and a suppo...
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Location
United Kingdom , Reading
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Senior Clinical Research Associate

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Join ICON plc as a Senior Clinical Research Associate in Johannesburg. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and participant safety. This role requires extensive CRA experience and a strong background in Respiratory studies, with 60% travel. We offer comp...
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Location
South Africa , Johannesburg
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