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630 Job Offers

Job Offers

Team Lead, Site Operations

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Lead a dedicated site operations team in Hickory, NC, as a Team Lead for ICON’s Accellacare network. This onsite role requires 3+ years of clinical site experience and strong leadership skills to oversee study start-up, maintenance, and close-out. You will drive quality, mentor staff, and collabo...
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United States , Hickory
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Talent Acquisition Business Partner

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ICON plc seeks a strategic Talent Acquisition Business Partner in Raleigh or Blue Bell, PA. You will drive full-cycle recruitment for healthcare and clinical research roles, leveraging data insights and ATS proficiency. This role demands strong stakeholder collaboration and a commitment to DEI. E...
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United States , Raleigh; Blue Bell
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Cra I

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Join ICON as a CRA I in Tel Aviv, Israel, and drive high-quality clinical trial monitoring. Leverage your ICH-GCP expertise and science degree to ensure patient safety and regulatory compliance. This role offers 60% travel, collaborative stakeholder engagement, and benefits like health insurance,...
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Israel , Tel Aviv
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Clinical Research Associate II

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ICON plc seeks a Clinical Research Associate II for a sponsor-dedicated Heart Failure (Cardiology) role based in Tbilisi, Georgia. You will conduct site monitoring visits, ensure ICH-GCP compliance, and safeguard data integrity. Requires 2+ years of CRA experience, a scientific degree, and 60% tr...
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Georgia , Tbilisi
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Clinical Quality Compliance Lead

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Lead Clinical Quality Compliance in Paris with ICON, a world-leading healthcare intelligence organization. You will manage compliance programs, oversee audits, and implement QMS to ensure regulatory alignment. Ideal for experts with a Bachelor's degree and proven experience in quality assurance w...
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France , Paris
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Global Study Associate

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Join ICON as a Site Management Associate I in São Paulo, Brazil. Support clinical trial site monitoring, ensure GCP compliance, and manage documentation. Ideal for candidates with a Bachelor’s in life sciences or clinical research and strong organizational skills. Enjoy benefits like annual leave...
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South Africa , Johannesburg
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Trial Delivery Management (Base)

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Lead and coordinate clinical trial projects as a Trial Delivery Manager at ICON in Blue Bell, PA. We seek a seasoned project management professional with a Bachelor’s degree and proven leadership skills to deliver results on time and within budget. Drive cross-functional teams, manage stakeholder...
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United States , Blue Bell
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Trial Delivery Management-Advanced

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Lead oncology clinical trials as a Trial Delivery Management Advanced at ICON in Burlington or Blue Bell, US. Drive project success with your extensive pharmaceutical project management expertise and leadership skills. Enjoy competitive benefits including health insurance, retirement planning, an...
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United States , Burlington; Blue Bell
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Trial Delivery Management (Base) - Immunology

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Lead and coordinate immunology trial delivery as a Trial Delivery Management (Base) at ICON in Blue Bell, PA. This role requires a Bachelor’s degree and proven project management expertise, driving timelines, budgets, and cross-functional teams. Leverage PMP or PRINCE2 certifications to ensure qu...
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United States , Blue Bell
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Contract Associate

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Join ICON plc as a Contract Associate in Madrid, Spain. Leverage your 2+ years of contract management experience and law/business degree to draft, negotiate, and manage agreements in a world-leading clinical research organization. Enjoy home-based flexibility, comprehensive health insurance, reti...
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Spain , Madrid
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Graduate Pharmacovigilance Associate

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Join ICON as a Graduate Pharmacovigilance Associate in Warsaw, Poland. Support global drug safety by collecting and processing adverse event data, preparing regulatory reports, and collaborating with cross-functional teams. Ideal for life science or pharmacy graduates with strong attention to det...
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Poland , Warsaw
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Medical Data Reviewer

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ICON plc seeks a Medical Data Reviewer in Warsaw, Poland. Leverage your Registered Nurse or life sciences background to ensure clinical data plausibility and consistency. You will independently draft Medical Data Review Plans and coordinate with Biometrics teams. Enjoy competitive benefits includ...
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Poland , Warsaw
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