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Senior Clinical System Designer

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Join ICON plc in Bangalore as a Senior Clinical System Designer. Lead end-to-end EDC study builds in Medidata Rave, ensuring high-quality database design and complex custom functions. Requires 5+ years of EDC experience and Rave proficiency. Enjoy competitive benefits including health insurance a...
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India , Bangalore
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Senior Data Scientist, Data Management

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Seeking a Senior Data Scientist specializing in Data Management for a remote US role. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient data linkage. This position offers competitive benefits and the chance to drive healthcare innovation with ICON p...
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United States , Raleigh, Blue Bell
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Program Manager, Clinical Data Science, Sponsor Dedicated

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Lead clinical data science programs at ICON, managing end-to-end project execution within scope and budget. Utilize your expertise in data science, statistics, and cross-functional leadership to drive clinical outcomes. This US-based role offers competitive health insurance, retirement planning, ...
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United States
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Senior Clinical Data Science Programmer

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Join ICON plc in Mexico City as a Senior Clinical Data Science Programmer. Utilize your advanced SAS, R, or Python skills to develop programming solutions for clinical trial data analysis and reporting. You will ensure data accuracy and efficiency in a collaborative, cross-functional environment....
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Mexico , Mexico City
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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 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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Visualisation Developer

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Join ICON plc as a Visualization Developer and shape the future of clinical development. Leverage your 4+ years of experience with Python, Spotfire, and clinical data (SDTM) to build advanced analytics solutions. Enjoy a supportive, innovative environment with competitive health insurance and ret...
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Senior Lead Clinical Data Science Programmer

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Lead advanced data science solutions for clinical trials at ICON plc. Utilize your expertise in SAS, R, or Python to ensure data integrity and support research. This senior role requires leadership skills and experience in clinical data programming. Enjoy competitive benefits including health ins...
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Clinical System Designer

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Join ICON plc, a global clinical research leader, as a Clinical System Designer I in Bangalore. You will design and implement clinical data management systems (CDMS) and eCRFs, ensuring they meet trial protocols and regulatory standards. This role requires functional knowledge of CDMS tools and t...
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India , Bangalore
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Senior Data Scientist, Data Management

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Seeking a Senior Data Scientist specializing in Data Management for an office-based role in Blue Bell, PA or Raleigh, NC. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient linkage methodologies. This role offers competitive benefits and the chance t...
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United States , Blue Bell, PA or Raleigh, NC
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Senior Statistical Programmer II

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Join ICON plc as a Senior Statistical Programmer II in Montreal (remote). Utilize your advanced SAS and R-Shiny skills to analyze clinical trial data, ensuring statistical integrity. This role offers competitive benefits and a chance to shape the future of clinical development within a global lea...
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Canada , Montreal
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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. Lead medical writing strategies for key clinical documents like protocols and CSRs. Utilize your 3-5+ years of CRO/pharma experience and regulatory knowledge in a dynamic, global team. Enjoy competitive benefit...
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