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Clinical Data Analyst

United States
Contract
Posted Today
Mid-Senior level
Remote
MLData ScienceAnalystMedical Equipment Manufacturing, Pharmaceutical Manufacturing, and Medical Practices

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Job Description

Job Title: Clinical Trial Data Analyst (Remote / Onsite - Princeton, NJ)

Contract Duration: 6+ Months


Location: Remote (Preference for candidates local to Princeton, NJ who can work onsite as needed)

Job Overview:

We are seeking a highly skilled Clinical Trial Data Analyst to support the operational feasibility, design, and analytics of clinical trial operations. This position involves working closely with cross-functional clinical teams to provide data-driven insights to optimize trial execution, site selection, and performance metrics.

Key Responsibilities:

  • Conduct feasibility assessments, site selection analytics, and study performance evaluations for clinical trials.
  • Perform data querying, aggregation, and analysis using Python and SQL.
  • Develop models that simulate clinical trial scenarios using Monte Carlo or other statistical techniques.
  • Utilize real-world data (RWD), including medical claims and electronic health records, to support trial planning.
  • Work with databases such as Citeline for trial benchmarking and study intelligence.
  • Present insights and findings clearly through Excel dashboards and PowerPoint presentations.
  • Collaborate with Clinical Operations and Data Science teams to provide recommendations and strategic input.

Required Qualifications:

  • Bachelor’s or Master’s degree in Data Science, Engineering, Computer Science, Statistics, or Machine Learning (experience may substitute for education).
  • 5+ years of experience in clinical trial analytics within a CRO or pharmaceutical company.
  • Strong understanding of clinical trial design, execution, and regulatory environment.
  • Proficiency in Python and SQL for data analysis.
  • Advanced skills in Excel and PowerPoint for data visualization and reporting.
  • Experience in modeling complex scenarios with multiple variables and outcomes (Monte Carlo Simulations preferred).
  • Familiarity with real-world data sources such as medical claims and EHRs.
  • Experience using clinical trial databases (e.g., Citeline) is a plus.

Source: LinkedIn
Over 200 applicants

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