IQVIA - Durham, NC

posted 3 months ago

Part-time
Durham, NC
Professional, Scientific, and Technical Services

About the position

The Spotfire Programmer position at IQVIA is a critical role within the data visualization team, focusing on the production of high-quality data visualizations and statistical outputs. This home-based position is open to candidates in the U.S. or Canada and requires recent experience with the Spotfire tool for data visualizations, particularly in creating dashboards for real-time data review. The role involves working closely with end users and internal colleagues to ensure that the visualizations meet the necessary standards and requirements. In this role, the Spotfire Programmer will be responsible for setting up studies and generating visualizations through Spotfire, preprocessing clinical data using SAS, and producing data visualizations using SAS, R, and R Shiny, all within the Spotfire environment. The position also requires assessing the quality of analysis data and performing cross-study analyses, which are essential for maintaining the integrity and accuracy of clinical trial data. Collaboration is key, as the programmer will work with Clinical Development teams to meet study deliverables and timelines, ensuring that all programming adheres to SDTM/ADaM specifications. Additionally, the Spotfire Programmer will assist in reviewing GSI Policies, SOPs, and other controlled documents, contributing to the continuous improvement of the Programming Environment. Participation in Programming and Biometrics meetings is also expected, providing input and insights that can enhance the overall programming processes. This position is ideal for someone with a strong background in clinical trial data and a passion for data visualization, looking to make a significant impact in the life sciences industry.

Responsibilities

  • Follow steps to set-up studies and generate visualizations through Spotfire.
  • Preprocess clinical data using SAS.
  • Produce data visualizations using SAS, R/R Shiny within the Spotfire tool.
  • Assess the quality of analysis data and perform cross-study analyses.
  • Collaborate with Clinical Development to meet study deliverables and timelines.
  • Familiarity with SDTM/ADaM programming specifications.
  • Assist in the review of GSI Policies, SOPs, and other controlled documents.
  • Collaborate with staff in Biostatistics, Clinical Data Management, and Clinical Research and Global Drug Safety.
  • Provide input to and participate in Programming and Biometrics meetings.
  • Contribute to the continuous improvement of the Programming Environment.

Requirements

  • 5 years or more of industry programming experience working with clinical trial data.
  • Bachelor's degree in biostatistics, computer science, biology, pharmacology, or related field.
  • Required work experience with the Spotfire tool.
  • Strong SAS programming proficiency is required.
  • Experience in R/R Shiny is strongly preferred.
  • Knowledge of clinical trial study design and electronic data submission requirements.
  • Sufficient understanding to follow the analysis plan and provide programming support for study deliverables.

Nice-to-haves

  • SQL programming skills.
  • Python programming skills.
  • Java programming skills.

Benefits

  • Incentive plans and bonuses based on performance.
  • Health and welfare benefits.
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