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9 часов назад

Head Benefit Risk and Pharmacoepidemiology

180 000 - 240 000
Формат работы
onsite
Тип работы
fulltime
Грейд
head
Английский
b2
Страна
France
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
Head Benefit Risk and Pharmacoepidemiology (Pharmacoepidemiology and Patient Safety): Leading epidemiology and benefit-risk strategies, studies, and evaluations for products across development and post-marketing with an accent on regulatory requirements, real-world data, and safety governance. Focus on building a high-performing multidisciplinary team, advancing analytical methods and tools, and shaping external policy through partnerships with regulators, academia, and industry.

Location: Gentilly, France; up to 25% travel may be required.

Salary: €180,000–€240,000 per year.

Company

hirify.global is a biopharmaceutical company developing medicines through patient-focused research, AI, data, and digital platforms.

What you will do

  • Define epidemiology and benefit-risk strategies for products across discovery, development, and post-marketing.
  • Oversee epidemiology safety studies, including PASS, to meet regulatory requirements.
  • Lead risk assessments and structured benefit-risk evaluations for senior safety governance bodies.
  • Manage and develop a multidisciplinary Epi & BR team, including capability building, career development, and budget management.
  • Develop rapid-access and analysis processes for real-world data used in safety evaluation.
  • Lead external collaborations, scientific partnerships, publications, presentations, and interactions with regulators and academia.

Requirements

  • Doctoral degree in biomedical sciences or public health, or an M.D. with an advanced degree in a related field.
  • At least 15 years of relevant professional experience with a Ph.D., or 12 years with an M.D.; at least 8 years in the pharmaceutical industry is preferred.
  • Experience in epidemiology, benefit-risk evaluation, risk management, signal detection and management, and patient safety sciences.
  • Leadership experience with large, diverse teams and external industry or public-private partnerships.
  • Strong statistics, biostatistics, quantitative analysis, real-world data, and regulatory guideline knowledge.
  • Scientific publication track record and experience across post-marketing and clinical development activities.

Culture & Benefits

  • Supportive, future-focused environment with international career development opportunities.
  • Health, wellbeing, prevention, and wellness benefits.
  • At least 14 weeks of gender-neutral parental leave.
  • Employee rewards and benefits programs.
  • Opportunity to work with AI, data, and digital platforms in drug discovery and development.

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