7 дней назад
Director, R&D Data Science & Digital Health, RWE & Advanced Analytics
164 000 - 282 900$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Director, R&D Data Science & Digital Health, RWE & Advanced Analytics (RWE/Advanced Analytics): Leading multidisciplinary teams in designing and delivering real-world evidence studies using observational databases, historical trial data, and literature reviews with an accent on bias mitigation, statistical analysis, and regulatory-grade evidence. Focus on developing external and hybrid control studies, creating study protocols and analysis plans, and translating findings for senior leaders and regulatory agencies.
Location: Hybrid role based in Titusville, New Jersey, United States of America; other listed job locations include Cambridge, Massachusetts, and Spring House, Pennsylvania.
Salary: $164,000–$282,900 base pay annually.
Company
Johnson & Johnson develops healthcare solutions and medicines through its Innovative Medicine and MedTech businesses.
What you will do
- Lead, manage, and mentor a multidisciplinary team of real-world evidence scientists.
- Build project roadmaps covering data feasibility, study design, analysis, and presentations to senior cross-functional leaders.
- Partner with Data Science Therapeutic Area leaders to develop and deliver real-world evidence strategies.
- Lead a portfolio of RWE projects and develop best practices and reusable tools for data scientists.
- Apply real-world data methodologies to external control arms, hybrid control studies, and comparative effectiveness analyses.
- Create study protocols, analysis plans, analytical datasets, tables, figures, and statistical programming deliverables.
Requirements
- Ph.D. in epidemiology or biostatistics.
- Good coding skills in R.
- At least 8 years of relevant experience in biopharma, RWE consulting, or healthcare industries.
- At least 5 years of experience as a people manager.
- Hands-on expertise in data analysis and statistical methods for mitigating confounding and selection biases.
- Experience with EHR, insurance claims, registry data, clinical trial data structures, and clear scientific communication.
Nice to have
- Expertise in drug development and experience in a matrixed organization.
- Subject matter knowledge in oncology.
- Experience producing regulatory-grade evidence and responding to agency reviews and comments.
Culture & Benefits
- Inclusive work environment focused on diversity, dignity, and equal opportunity.
- Eligibility for pension and 401(k) savings plans.
- Participation in a long-term incentive program.
- Paid vacation, sick time, holidays, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time off.
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