5 дней назад
Real World Evidence Strategy Lead
206 250 - 297 917$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Real World Evidence Strategy Lead (RWE/AI-powered biopharma): Establishing and executing real-world evidence strategies and studies across global therapeutic areas with an accent on pharmacoepidemiology, health economics, regulatory evidence, and real-world data. Focus on designing rigorous studies, translating medical needs into evidence requirements, managing end-to-end execution, and applying AI-powered analytics to support clinical, regulatory, reimbursement, and launch decisions.
Location: Hybrid in Morristown, New Jersey or Cambridge, Massachusetts; US and Puerto Rico residents only
Salary: $206,250–$297,916.66 annually
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines through immunoscience, real-world evidence, data, and digital platforms.
What you will do
- Establish asset and brand real-world evidence strategies aligned with global disease-area, medical, regulatory, access, and lifecycle objectives.
- Translate medical needs into fit-for-purpose evidence requirements and integrated evidence generation plans.
- Develop data strategies by assessing the availability, access, and suitability of claims databases, electronic medical records, registries, and other healthcare data sources.
- Design and execute innovative real-world studies using advanced methodologies, analytics, AI, digital platforms, and internal or external expertise.
- Lead end-to-end study delivery, including budgets, timelines, quality, reporting, publications, and regulatory or reimbursement submissions.
- Partner with Medical, Market Access, HEVA, Global Brand Teams, regulators, vendors, and scientific stakeholders to align evidence plans and communicate insights.
Requirements
- Advanced degree in pharmacoepidemiology, biostatistics, health outcomes, or an equivalent discipline; PhD preferred.
- At least 10 years of real-world evidence generation experience in or for the pharmaceutical industry.
- End-to-end leadership of real-world studies from concept through completion and publication for regulatory or reimbursement submissions.
- Expertise in pharmacoepidemiology, HEOR, RWE study design and methodology, routinely collected healthcare data, and innovative analytics.
- Demonstrated peer-reviewed publication record in epidemiology, clinical, statistical, and/or HEOR journals.
- Fluent spoken and written business English is mandatory; the role is hybrid in the United States and available to US and Puerto Rico residents only.
Nice to have
- Experience in immunology, rare diseases, oncology, neurology, or ophthalmology.
- Formal education in business or management.
- Proficiency or working knowledge of French or another European language.
Culture & Benefits
- Work in a supportive, future-focused R&D environment centered on scientific innovation and patient outcomes.
- Opportunities for promotion, lateral career development, and international growth.
- Company rewards package with healthcare, wellness, prevention, and family benefits.
- At least 14 weeks of gender-neutral parental leave.
- Access to cutting-edge AI, data, and digital platforms for drug discovery and evidence generation.
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