Senior SAS Programmer for Clinical Trials

4 weeks ago


Washington, United States IQVIA Full time

Job Description

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This Senior SAS Programmer for Clinical Trials position will be responsible for developing and implementing statistical programs for clinical trials, providing technical expertise, and leading teams.

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Responsibilities:

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  • Develop and implement statistical programs for clinical trials.">
  • Provide technical expertise to internal and external clients.">
  • Lead teams and manage resources to achieve project goals.">
  • Maintain relationships with internal and external stakeholders to ensure successful project delivery.">
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Requirements:

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  • Bachelor's degree in science or mathematics-related fields.">
  • Minimum 4+ years of experience in Statistical Programming in pharmaceutical or medical devices industry.">
  • Expertise in SAS programming, R, and CDISC standards.">
  • Strong communication, leadership, and problem-solving skills.">
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Compensation: $117,400 - $218,000 per year, based on qualifications and location.

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About IQVIA

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IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments.



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