About The Position

IQVIA is hiring to expand a sponsor-dedicated team, working fully within the environment of a prominent Pharma company. The position will work in a data visualization team, safety statistical programming. The statistical 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.

Requirements

  • 4 years or more of industry programming experience, along with a bachelor’s degree in biostatistics, computer science, biology, pharmacology or related.
  • Proficient in data visualization software – Spotfire.
  • Demonstrates SAS programming proficiency.
  • 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, Python and Java programming skills is nice to have experience.

Responsibilities

  • Programs visualization analysis datasets using SAS.
  • Assesses the quality of analysis data and performs cross-study analyses.
  • Works collaboratively with Clinical Development to meet study deliverables and timelines.
  • Creation and updates for SDTM/ADaM programming specifications.
  • Follow the steps to set-up studies using Spotfire.
  • 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.
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