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Senior Clinical Research Associate

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Location
South Korea , Seoul
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Not provided
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Drug Safety Associate

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South Korea , Seoul
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Senior Validation Engineer

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Join ICON plc as a Senior Validation Engineer in Blue Bell, PA or Raleigh, NC. This office-based role with remote flexibility requires 10+ years of CSV/GxP experience. You will lead validation for complex global projects, ensuring compliance with FDA and EMA regulations. We offer competitive heal...
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United States , Blue Bell, PA or Raleigh, NC
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Senior Clinical Research Associate

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United States , Los Angeles; San Francisco; San Diego; Portland; Salt Lake City
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110520.00 - 138150.00 USD / Year
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Director, Bioanalytical Services

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United States , Lenexa
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Clinical Research Site Project Manager

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United States
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Clinical Data Validation Engineer Specialist

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Join ICON as a Senior Clinical Data Science Programmer in Bangalore. Utilize your SAS/R/Python expertise to develop programming solutions for clinical trial data analysis and reporting. Collaborate cross-functionally to ensure data accuracy and support innovative therapies. Enjoy competitive bene...
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India , Bangalore
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Senior Clinical Research Associate

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New Zealand , Wellington or Auckland
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Regulatory Submissions Manager

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Lead regulatory submissions (CTA/IND/MAA) for a global pharmaceutical sponsor in this home-based role in Australia. Leverage 6+ years of pharmaceutical regulatory affairs experience to provide strategic guidance and lead internal teams. Enjoy a competitive package with health insurance and a supp...
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Australia , Sydney
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Manager, Clinical Operation

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Lead clinical trials from planning to execution in Taipei, Taiwan. This pivotal role requires extensive operations management experience and strong leadership skills to ensure regulatory compliance and trial efficiency. You will mentor teams and drive innovation in a world-leading clinical resear...
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Taiwan , Taipei
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Clinical Research Project Associate

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United States , Lenexa
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Head of HR Technology (Workday)

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Ireland , Dublin
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