Senior Statistical Programmer, Spotfire Data Visualization

Location: home-based in the U.S. or Canada

Summary: This job requires recent working experience with the Spotfire tool for data visualizations, creating dashboards for real time data review. Also, this job requires strong SAS programming skills and industry experience working with clinical trial data.

IQVIA is hiring to expand a data visualization team, offering long-term dedication to a prominent Pharma company. The position will work in a data visualization team, safety statistical programming. The Spotfire Programmer works collaboratively with the end users, internal colleagues to ensure the high-quality production of data visualizations and statistical outputs using Spotfire/R and other visualization tools. Support real-time online clinical trial data review.

Job responsibilities:

• Follow steps to set-up studies and generate visualizations through Spotfire.
• Preprocessing clinical data using SAS.
• Producing data visualizations using SAS, R/R Shiny - all within the Spotfire tool.
• Assesses the quality of analysis data and performs cross-study analyses.
• Works collaboratively with Clinical Development to meet study deliverables and timelines.
• Familiarity following SDTM/ADaM programming specifications.
• Assist in the review of GSI Policies, SOPs and other controlled documents.
• Collaboration 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 Programming Environment.
  
  

Qualifications:

• 5 years or more of clinical trials industry programming experience, must have experience working with clinical trial data.
• Bachelor’s degree in biostatistics, computer science, biology, pharmacology or related.
• Required to have recent work experience with Spotfire tool.
• Strong SAS programming proficiency is required.
• Strongly preferred to have experience in R/R Shiny.
• 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.
  
  

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

The potential base pay range for this role, when annualized, is $106,200.00 - $177,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.