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5 дней назад

Regulatory and Start Up Specialist with Contracts - Hungary (Clinical Research)

Формат работы
remote (только Hungary)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Hungary
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
Regulatory and Start Up Specialist with Contracts - Hungary (Clinical Research): Coordinating clinical trial site activation, regulatory submissions, essential documents, and contract activities in Hungary with an accent on local regulatory compliance, clinical trial agreements, and stakeholder coordination. Focus on managing submission and approval timelines, reviewing site documentation, identifying project risks, and supporting successful study start-up delivery.

Location: Home-based within Hungary; the posting also lists Budapest, Hungary.

Company

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

What you will do

  • Act as the primary contact for investigative sites, Site Activation Managers, project managers, sponsors, and internal stakeholders.
  • Coordinate country-specific site activation and regulatory activities for clinical studies.
  • Prepare, review, distribute, and track regulatory and essential study documentation, including ethics submissions, informed consent forms, investigator pack documentation, and clinical trial agreements.
  • Support contract negotiation activities and monitor submission, approval, execution, and project milestones.
  • Identify risks and mitigation plans, perform quality reviews, and maintain accurate records in internal tracking systems.
  • Provide local regulatory expertise and contribute to process improvement and successful study start-up delivery.

Requirements

  • Bachelor’s degree in life sciences or a related scientific discipline.
  • Approximately 3.5–5 years of experience in clinical research.
  • Strong experience with site activation, regulatory submissions, clinical trial agreements, contract negotiations, and clinical trial start-up activities.
  • Strong understanding of Hungarian and international clinical trial regulations.
  • Fluent Hungarian is essential.
  • Strong English communication skills are required. Excellent planning, organization, problem-solving, stakeholder management, and communication abilities are also expected.

Culture & Benefits

  • Home-based flexibility within Hungary.
  • Opportunity to support innovative clinical studies across a range of therapeutic areas and sponsors.
  • Global career development and advancement opportunities.
  • Collaborative and inclusive environment focused on growth and continuous learning.
  • Work supporting healthcare innovation and improved patient outcomes.

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