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Senior Clinical Research Associate

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United States , Chicago
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Study Start Up Associate II

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South Korea , Seoul
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Heor scientist

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United States , RALEIGH, BLUE BELL, BASKING RIDGE, NJ, CHICAGO, IL, SEATTLE, WA, DALLAS, TX, HOUSTON, TX
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Clinical Outcomes Assessment Analyst

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United States , CARY, BLUE BELL, INDIANAPOLIS, MIAMI, TAMPA, DALLAS, HOUSTON
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Clinical Budget Analyst

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Join ICON plc as a Clinical Budget Analyst in Blue Bell. Develop and analyze pricing strategies for clinical trials, ensuring financial accuracy and cost optimization. This role requires financial analysis expertise and offers competitive benefits including health insurance and retirement planning.
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United States , Blue Bell
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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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Senior Medical Writer

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Join ICON plc as a Senior Medical Writer and shape the future of clinical development. You will lead medical writing strategies for clinical research, producing high-quality protocols, CSRs, and regulatory documents. This role requires 3-5 years of experience in a CRO/pharma setting and expertise...
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Clinical Research Associate II

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Join ICON plc as a Clinical Research Associate II in Bratislava. You will monitor clinical trial sites, ensure GCP compliance, and manage data integrity. This role requires 3-6 years of CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retiremen...
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Slovakia , Bratislava
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Feasibility Strategy & Analytics Lead

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Lead our clinical trial feasibility strategy in Reading. Develop data-driven country and site plans to optimize patient recruitment and study delivery. Requires 7+ years in clinical research, drug development knowledge, and strong analytical skills. We offer competitive health insurance, retireme...
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United Kingdom , Reading
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Regulatory Submissions Manager

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Lead regulatory submissions and strategy for drug development at a global CRO. This role in Yerevan requires 6+ years of pharma/biotech experience, including CTA/IND/MAA filings. You will provide expert guidance, manage agency interactions, and ensure compliance. We offer competitive benefits inc...
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Armenia , Yerevan
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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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