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5 дней назад

Real World Evidence Strategy Lead

206 250 - 297 917$
Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
Английский
c1
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Текст:
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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

hirify.global 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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