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13 дней назад

Medical Evidence Development Asset Lead (Real-World Evidence)

140 200 - 390 600$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Medical Evidence Development Asset Lead (Real-World Evidence): Leading integrated evidence generation plans and their execution for life sciences assets, with an accent on real-world evidence, observational research, and oncology development. Focus on coordinating cross-functional stakeholders, guiding study design and regulatory-grade evidence projects, and mitigating research delivery risks.

Location: Durham, North Carolina, United States of America

Annual base pay: $140,200–$390,600

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Support and oversee integrated evidence generation plans for assigned assets.
  • Coordinate epidemiology, real-world evidence, patient-centered research, statistics, regulatory, safety, operations, and access stakeholders.
  • Lead cross-functional meetings and oversee tactical implementation, study progress, metrics, and resourcing.
  • Advise on evidence generation strategy, study design, and innovative real-world evidence approaches.
  • Review critical regulatory and study-level documents and represent assets in enterprise and therapeutic-area initiatives.
  • Identify and mitigate risks affecting medical affairs research delivery.

Requirements

  • Direct experience developing and executing integrated evidence generation plans; at least 1 year required, with 3 or more years preferred.
  • Advanced science degree and significant professional experience in real-world evidence and life sciences.
  • Expert knowledge of drug and oncology development processes.
  • Experience with real-world evidence, observational, and low-interventional study designs.
  • Experience supporting regulatory-grade real-world evidence projects and contributing to regulatory interactions or correspondence.
  • Strong communication, organizational, project management, analytical, decision-making, and stakeholder relationship skills.

Culture & Benefits

  • Full-time employment within a global clinical research and healthcare intelligence organization.
  • Collaboration with senior stakeholders and multidisciplinary teams across life sciences functions.
  • Health and welfare benefits may be available in addition to the base pay range.
  • Incentive plans, bonuses, or other compensation may be offered depending on the position.

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