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2 дня назад

Real-World Evidence Project Manager

Формат работы
remote (только Europe)
Тип работы
fulltime
Английский
b2
Страна
France/Germany
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
Real-World Evidence Project Manager (Clinical Research/Remote Monitoring): Leading end-to-end real-world evidence studies in France and Germany, covering protocols, ethics submissions, data collection, budgets, sites, CROs, and sponsor deliverables with an accent on oncology, haematology, and healthcare data. Focus on coordinating clinical and non-interventional studies, managing risks and research partners, and assessing clinical data quality and AI-assisted extraction.

Location: Remote in France or Germany; listed locations include Paris, Biarritz, Bordeaux, Lyon, Marseille, Munich, Nantes, Rennes, and Toulouse.

Company

hirify.global is a French health technology company founded in 2021 that develops remote medical monitoring solutions and supports clinical research through patient-reported outcomes, AI technologies, and real-world data.

What you will do

  • Lead clinical and non-interventional real-world evidence studies from contracting through final reports.
  • Coordinate protocols, statistical analysis plans, ethics submissions, data collection, and study deliverables.
  • Manage timelines, risks, budgets, site costs, and clinical research organisation costs.
  • Select and activate research sites, coordinate contracting, and oversee CRO partners.
  • Act as the primary operational contact for sponsors and lead steering committees with international pharmaceutical partners.
  • Collaborate with Medical, Clinical Operations, Data, Legal, and Quality teams to develop reusable study methods.

Requirements

  • Experience leading clinical or non-interventional studies with direct responsibility for timelines and deliverables.
  • Experience working with investigator sites and research partners in the French or German research environment.
  • Knowledge of ethics committees, GDPR/DSGVO, Länder-level data protection requirements, hospital contracting, pharmacovigilance, and monitoring plans.
  • Experience overseeing CROs from the sponsor side and tracking study budgets and costs.
  • Ability to assess clinical data quality and discuss electronic health record structuring and AI-assisted extraction.
  • Professional English fluency in written and spoken communication is required.

Nice to have

  • Experience delivering studies in oncology or haematology.
  • Experience combining remote monitoring, patient-reported outcomes, and clinical data.

Culture & Benefits

  • Autonomous ownership of projects with clear priorities and decision-making support.
  • International and distributed collaboration across multidisciplinary teams.
  • Focus on early communication, practical solutions, reliable execution, and continuous process improvement.
  • Opportunity to contribute to personalized medicine, real-world evidence, and clinical research.

Hiring process

  • 15-minute screening interview focused on motivation and role prerequisites.
  • 30-minute manager-fit interview, followed by a business case presentation and Q&A.
  • Team-fit and strategic-fit interviews with cross-functional colleagues.

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