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3 дня назад

Medical Affairs Research Manager (Pharmaceutical Research)

Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
US/Netherlands
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 Affairs Research Manager (Pharmaceutical Research): Managing medical research projects and multi-country observational studies in the Netherlands with an accent on compliant study execution, site coordination, budget oversight, and regulatory documentation. Focus on coordinating Ethics Committee submissions, negotiating study agreements and site budgets, tracking deliverables, and improving research processes across affiliate and international teams.

Location: Hybrid position with office location in Hoofddorp, Netherlands

Company

hirify.global develops innovative medicines and solutions across immunology, oncology, neuroscience, and Allergan Aesthetics.

What you will do

  • Act as the primary contact for designated medical research projects across affiliate medical teams and therapeutic areas.
  • Support the feasibility, setup, and compliant delivery of local studies and multi-country observational studies.
  • Coordinate research proposals, study tracking, documentation, Ethics Committee submissions, and regulatory audit preparation using systems including SPIRIT, Veeva Vault Clinical, and TESLA.
  • Collaborate with medical advisors, medical science liaisons, investigators, site staff, legal teams, and other stakeholders on site selection, visits, contracts, and study close-out.
  • Manage budget negotiations, Clinical Study Agreement negotiations, invoice tracking, study drug shipments, and project status reporting.
  • Improve project management processes, systems, and user experience for medical research projects in the Netherlands.

Requirements

  • Bachelor’s or master’s degree in life science or a related discipline.
  • At least three years of industry-based pharmaceutical clinical research experience.
  • Strong knowledge of clinical trial legislation, regulations, and operational requirements.
  • Extensive project management experience with study management, documentation, budget tracking, and stakeholder coordination.
  • Fluent Dutch and English, both written and spoken.
  • Excellent proficiency with Microsoft Office and other IT tools, alongside a high standard of ethics, compliance, and professional integrity.

Culture & Benefits

  • Hybrid work arrangement based in Hoofddorp.
  • Work across affiliate, area, and international medical teams.
  • Opportunity to contribute to innovative medicines and solutions for serious health issues.
  • Equal opportunity employment with an emphasis on integrity, innovation, and community impact.

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