Department Specific Responsibilities

      • Qualitative studies (e.g., interviews and focus groups)
      • Quantitative studies (e.g., patient/provider surveys, cross-sectional and longitudinal designs)
      • Hybrid studies (e.g., qualitative plus quantitative, survey augmented with claims)
      • Patient preference studies
      • Direct to patient studies (no site involvement)
      • Risk Evaluation and Mitigation Studies (REMS)
      • Panel studies
      • Guideline studies
      • Value-based studies

Minimum Requirements

  • Requires a MS, PhD, or equivalent in epidemiology, biostatistics, health services research, or related field.
  • 10+ years’ experience in the field of epidemiology, clinical research and/or health services research.
  • Prior experience working with the biopharmaceutical industry, federal regulatory agencies and/or payer organizations preferred.
  • Strong patient-centered research background in qualitative and quantitative research designs that include study methodology and analytical skills, ideally with knowledge of pre-approval and/or post-approval research studies.
  • Prior experience working with healthcare claims data preferred.
  • Record of publication in peer-reviewed scientific journals preferred.
  • Relevant experience in conducting research using health plan administrative claims databases (pharmacy and medical claims) preferred.
  • Excellent oral, written, and presentation skills.
  • Ability to thrive in a constantly changing environment.

Tagged as: Principal Scientist

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