RWE Specialist

Remote – UKFull-TimeMiddle
Salary not disclosed
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Job Details

Experience
3–5 years
Required Skills
PythonSQLR

Requirements

  • Advanced degree in Epidemiology, Biostatistics, Public Health, or related field preferred
  • 3–5 years of relevant experience in real-world data analytics or related field
  • Proficiency in SAS
  • Proficiency in R
  • Proficiency in Python
  • Proficiency in SQL
  • Experience working with healthcare data sources including EHRs, claims, and registries
  • Strong understanding of clinical trial design and real-world evidence methodologies
  • Demonstrated ability to develop and apply innovative analytical tools and approaches
  • Excellent communication and collaboration skills
  • Ability to work independently and cross-functionally in a fast-paced, matrixed environment

Responsibilities

  • Understand and be familiar with licensed RWD database(s) relevant to clinical research initiatives
  • Independently identify, access, and assess in-house real-world data sources (EHRs, claims, registries, etc.)
  • Access and summarize non-patient-level real-world data (publications, aggregate claims or EHR analytics, federated learnings, external collaborations, etc.)
  • Critically evaluate data quality, completeness, and suitability for specific trial design questions
  • Develop RWD exploration plans
  • Clean, process, and harmonize raw RWD for analysis, applying data governance and privacy standards
  • Use SAS, R, Python and/or other advanced analytical programming tools to perform statistical analyses and generate insights
  • Prepare clear, concise evidence summaries and visual reports to inform protocol development
  • Collaborate cross-functionally with clinical, regulatory, biostatistics, and medical teams
  • Stay current on RWD methodologies, regulatory guidance, and technological advances
  • Ensure all work supports timely, high-quality decision making for new clinical trial design and execution
  • Develop innovative RWD analytical tools to support evolving clinical trial needs
  • Conduct independent assessments of data sources to determine relevance, quality, and utility
  • Incorporate input from internal subject matter experts (SMEs) to ensure alignment with RWE/RWD best practices and strategic objectives
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