Senior Manager, RWE & Epidemiology Strategy

Boston Scientific; Arden Hills (MN); Hybrid; USD 126,000 - 239,000; Full time

Job summary

Boston Scientific seeks a Senior Manager, Clinical Real-World Evidence Strategist in Epidemiology to lead enterprise RWE initiatives and work with Clinical, Regulatory, Medical Affairs, and Biostatistics to translate clinical questions into robust RWE programs.

You will design observational studies using claims, EHR, registries, and other real-world data sources, develop protocols and analysis plans, and publish results to support regulatory, reimbursement, and product decisions.

Qualifications

• Bachelor’s or advanced degree in Epidemiology, Clinical Research, Biostatistics, Public Health or related discipline.
• Minimum of 7 years of experience in clinical research, epidemiology, biostatistics, outcomes research or real-world evidence.
• Strong expertise in epidemiology and observational methods including cohort studies and causal inference.
• Experience developing protocols, analysis plans, and publication plans with clinical and biostatistical teams.

Responsibilities

• Lead enterprise RWE initiatives and provide methodological expertise in study design and interpretation.
• Collaborate with physicians, Clinical Affairs, Medical Affairs, Regulatory Affairs, and Biostatistics to translate clinical questions into RWE studies.
• Design observational studies using claims, EHR, registries, and other real-world data sources.
• Develop and review study concepts, protocols, statistical analysis plans, and publication strategies.
• Guide epidemiologic concepts, bias assessment, missing data, and causal inference to ensure valid results.

Skills

Epidemiology

Observational research

Biostatistics

Scientific communication

Study design

Education

PhD / DrPH / ScD / MD / MPH / MS or equivalent

Tools

R

SAS

Python

SQL

Job description

Boston Scientific seeks a Senior Manager, Clinical Real-World Evidence Strategist in Epidemiology to lead enterprise RWE initiatives and work with Clinical, Regulatory, Medical Affairs, and Biostatistics to translate clinical questions into robust RWE programs.

You will design observational studies using claims, EHR, registries, and other real-world data sources, develop protocols and analysis plans, and publish results to support regulatory, reimbursement, and product decisions.