4 часа назад
Associate Director, Market Access Analytics and Real World Evidence (MAA & RWE) – Indirect Treatment Comparisons
137 000 - 235 750$
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Описание вакансии
Текст:
TL;DR
Associate Director, Market Access Analytics and Real World Evidence (Indirect Treatment Comparisons) (Market Access Analytics/RWE): Designing and delivering market access analytics and evidence-generation workstreams for payer and regulatory requirements with an accent on indirect treatment comparisons, comparative effectiveness research, and advanced statistical methods. Focus on developing HTA and payer submission evidence, analyzing clinical and real-world data, and coordinating cross-functional research delivery.
Location: Based in Raritan, New Jersey, United States, or Beerse, Belgium; up to 10% travel may be required.
Salary: $137,000–$235,750 annual base pay in the United States, plus eligibility for an annual performance bonus.
Company
Johnson & Johnson MedTech is a healthcare innovation company developing medical and pharmaceutical solutions across complex diseases and patient care.
What you will do
- Design and conduct market access analytics aligned with payer and regulatory evidentiary requirements.
- Lead indirect treatment comparisons, including MAIC, STC, NMA, and ML-NMR, as well as observational and comparative effectiveness studies.
- Direct end-to-end evidence-generation workstreams covering systematic literature reviews, feasibility assessments, protocols, statistical analysis plans, reports, and publications.
- Apply regression, mixed-effects, survival, propensity score, and non-parametric methods according to study protocols.
- Partner with Global Market Access, R&D, Medical Affairs, Health Economics Modeling, and Epidemiology teams on evidence-generation strategies.
- Provide scientific and technical input to external research partners and support HTA and payer submissions.
Requirements
- Master’s degree or higher in biostatistics, mathematics, computational sciences, economics, public health, health administration, operations research, or a related field.
- At least 6 years of relevant experience, or at least 4 years with a doctoral degree, in pharmaceutical, biotech, or consulting environments.
- Demonstrated experience with indirect treatment comparisons and comparative effectiveness research, preferably for HTA submissions and publications.
- Proficiency in statistical programming with R, SAS, and other relevant tools.
- Experience analyzing clinical trial data, systematic literature review data, administrative claims, electronic health records, and clinical registries.
- Strong project management, organizational, communication, and prioritization skills.
Culture & Benefits
- Inclusive work environment guided by the company’s Credo and focused on employee dignity and diversity.
- Eligibility for pension, 401(k), savings, and long-term incentive programs under applicable plans.
- Paid vacation, sick time, holidays, personal and family time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time off.
- Up to 10% travel may be required.
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