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Senior clinical data coordinator

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Join ICON plc as a Senior Clinical Data Coordinator in Mexico City. Utilize your 5-7 years of experience with RAVE or Veeva to ensure data quality and regulatory compliance. You will develop data management plans, mentor junior staff, and collaborate with cross-functional teams. We offer competit...
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Location
Mexico , Mexico City
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Not provided
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Regulatory Affairs Manager

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Lead regulatory submissions and strategy as a home-based Manager in Seoul. Utilize 6+ years of pharmaceutical regulatory experience to guide drug development from CTA to post-approval. Enjoy competitive benefits including health insurance and global support, driving excellence at a world-leading ...
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South Korea , Seoul
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Not provided
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Clinical Trial Administrator

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Join ICON plc as a Clinical Trial Administrator in Mexico City. Support the design and analysis of clinical trials, ensuring protocol compliance and managing essential documentation. This role requires a scientific degree, knowledge of trial processes, and strong organizational skills. We offer c...
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Mexico , Mexico City
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Not provided
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Project Manager

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Lead clinical research projects from home in Brazil for a global healthcare leader. Utilize your project management expertise to deliver high-quality results on time and within budget. Enjoy competitive benefits including health insurance and retirement planning. Join ICON plc to shape the future...
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Location
Brazil , Sao Paulo
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Clinical Trial Manager

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Join ICON plc as a Senior Clinical Trial Manager in a home-based role in Brazil. You will ensure successful study delivery, manage budgets, and drive enrollment for global trials. This sponsor-dedicated position requires extensive CRO/pharma experience and offers competitive health insurance and ...
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Brazil , Sao Paulo
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Not provided
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Research Operations Coordinator

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Join ICON plc, a global clinical research leader, as a Research Operations Coordinator in the United States. Support project execution and clinical trial coordination within the pharmaceutical industry. Utilize your organizational skills and life sciences background in a dynamic team. Enjoy compe...
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United States
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Not provided
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Global Study Manager

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Seeking a Global Study Manager with 3+ years in clinical trial management, including phase I oncology. You will oversee global study execution, vendor management, and key document development. This remote US role (Eastern/Central time) offers competitive health insurance and retirement benefits a...
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Location
United States
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Not provided
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Senior Manager, Procurement- IVRS

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Lead strategic procurement for clinical trials as a Senior Manager at ICON. Utilize your IVRS expertise and healthcare sourcing background to drive cost efficiencies and supplier relationships. This US-based role offers competitive benefits, focusing on data-driven decisions and cross-functional ...
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United States
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Medical Research Associate

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Join ICON plc, a global clinical research leader, as a Medical Research Associate in San Antonio. This role is ideal for an ACLS-certified Paramedic/EMT to conduct vitals checks, phlebotomy, and screen participants. We offer competitive pay, comprehensive health insurance, and a flexible benefits...
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United States , San Antonio
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Not provided
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Set Up Specialist

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Join ICON plc, a global clinical research leader, as a Set Up Specialist. You will coordinate clinical trial setup, ensuring regulatory compliance and efficient study execution. This role requires a life sciences degree and experience in trial setup or site management. The position offers competi...
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United States , Farmingdale, NY, Blue Bell PA or Raleigh NC
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Scientist II

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Join our winning lab team at ICON plc, a top-rated employer. We seek a Scientist II in Whitesboro, NY to develop and perform GLP/GCP assays for clinical trials. The role requires a Bachelor's in Biology/Chemistry and experience with binding assays. We offer a competitive salary, bonus, and compre...
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United States , Whitesboro
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Salary
56704.00 - 70880.00 USD / Year
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Senior Clinical Research Associate

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Join ICON plc as a Senior Clinical Research Associate in Copenhagen. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive benefits including health ins...
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Denmark , Copenhagen
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Not provided
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