7 дней назад
Senior Principal Scientist, Data Science RWE (Real-World Evidence)
137 000 - 235 750$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Senior Principal Scientist, Data Science RWE (Real-World Evidence): Leading real-world evidence projects and developing statistical and programming methods for external control arms, hybrid controls, comparative effectiveness analyses, and post-hoc clinical trial analyses with an accent on RWE study design, bias mitigation, and regulatory-grade evidence. Focus on building reusable tools, creating study protocols and statistical analysis plans, analyzing healthcare data sources, and mentoring data scientists.
Location: Hybrid role based in Titusville, New Jersey, United States of America. Additional posting locations include Cambridge, Massachusetts; Raritan, New Jersey; and Spring House, Pennsylvania.
Salary: $137,000–$235,750 per year, plus eligibility for incentive, retirement, and paid-leave programs.
Company
Johnson & Johnson MedTech and Innovative Medicine develop healthcare treatments, technologies, and solutions across the spectrum of patient care.
What you will do
- Lead a portfolio of real-world evidence projects as a hands-on scientific and technical leader.
- Develop best practices and maintain reusable tools that accelerate real-world data science delivery.
- Design and execute end-to-end RWE studies, including research questions, feasibility, study design, analysis, programming, and interpretation.
- Develop methods to mitigate observed and unobserved bias in external control arm, hybrid control, and comparative effectiveness studies.
- Generate actionable insights from post-hoc RCT analyses, observational databases, and literature reviews for regulatory interactions.
- Partner with therapeutic-area data scientists, mentor team members, and deliver protocols, statistical analysis plans, analysis-ready data, tables, and figures.
Requirements
- Ph.D. in epidemiology or biostatistics.
- Expert coding skills in R, Python, or SAS.
- At least 5 years of relevant experience in biopharma, RWE consulting, or related healthcare industries.
- Hands-on experience extracting, cleaning, and analyzing data, including methods for mitigating confounding and selection bias.
- Expertise with multiple real-world data sources, including EHR, insurance claims, and registry data; familiarity with clinical trial data structures.
- Excellent interpersonal, communication, presentation, and mentoring skills.
Nice to have
- Familiarity with drug discovery and clinical development.
- Subject matter knowledge in oncology, immunology, or neuroscience.
- Experience producing regulatory-grade evidence and responding to agency reviews and comments.
Culture & Benefits
- Inclusive work environment guided by the company’s Credo and equal opportunity principles.
- Retirement pension and 401(k) savings plans.
- Long-term incentive program eligibility.
- Paid vacation, sick time, holidays, personal and family time, parental, bereavement, caregiver, volunteer, and military spouse leave.
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