RWE Lead Scientist — Observational Data & Regulation

Scorpion Therapeutics

Spring House (PA)

On-site

USD 180,000 - 240,000

Full time

14 days+
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Job summary

Johnson & Johnson's Innovative Medicines division seeks a Lead scientific and technical expert in Real-World Evidence (RWE) to oversee RWE projects, develop methodologies, and mentor team members.

You will lead end-to-end RWE studies, design analytic plans, create tools to streamline delivery, mitigate bias in external control studies, and collaborate with therapy area scientists to inform regulatory interactions with real-world data sources such as EHRs and claims databases.

Qualifications

  • Ph.D. in epidemiology or biostatistics required.
  • Minimum 5 years' relevant experience in biopharma or healthcare data analytics.
  • Expert coding skills in R, Python, or SAS.
  • Extensive experience with real-world data sources (EHR, claims, registries).
  • Proficiency in statistical bias mitigation techniques.
  • Strong communication skills.

Responsibilities

  • Lead end-to-end RWE studies including data feasibility, study design, analysis, and interpretation.
  • Develop tools to streamline project delivery.
  • Provide thought leadership on bias mitigation in external control and comparative studies.
  • Generate insights from post-hoc RCT analyses and observational data to support regulatory interactions.
  • Create study protocols and statistical analysis plans.
  • Collaborate with therapeutic area scientists to shape RWE strategies.

Skills

R
Python
SAS

Education

Ph.D. in epidemiology or biostatistics

Tools

EHR data
Claims data
Registries

Job description

Johnson & Johnson's Innovative Medicines division seeks a Lead scientific and technical expert in Real-World Evidence (RWE) to oversee RWE projects, develop methodologies, and mentor team members.

You will lead end-to-end RWE studies, design analytic plans, create tools to streamline delivery, mitigate bias in external control studies, and collaborate with therapy area scientists to inform regulatory interactions with real-world data sources such as EHRs and claims databases.

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