Назад
Company hidden
7 дней назад

Senior Manager, Global Site Activation, Legal Liaison

201 500 - 374 100PLN
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Poland
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
Senior Manager, Global Site Activation, Legal Liaison (Clinical Research and Site Contracting): Providing operational support and guidance for clinical trial contracting, with an accent on contract templates, legal alignment, and country-specific requirements. Focus on resolving complex contracting issues, standardizing site contracting practices, and applying GCP/ICH and regulatory guidelines across EU clinical research activities.

Location: Warsaw, Poland

Annual base pay: PLN 201,500–374,100

Company

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

What you will do

  • Provide study-specific contracting support to Project Managers, SSUMs, Site Contract Negotiators, and Global Template Developers.
  • Serve as the primary operational contact for complex contracting issues and escalate legal matters to the Legal Department when appropriate.
  • Advise stakeholders on approved contracting positions, templates, and contracting policies.
  • Own and maintain the Global Site Contracts Library, including country-specific templates, guidance documents, and supporting materials.
  • Lead contract template development, validation, maintenance, translation coordination, version control, and continuous improvement.
  • Train and support Site Contracts teams while driving standardization, compliance, and operational excellence.

Requirements

  • Master’s degree in law and demonstrable experience as a qualified lawyer.
  • At least 5 years of relevant sponsor or clinical research organization experience in clinical site contracting.
  • Demonstrable experience acting as an EU legal contract expert.
  • Strong negotiation, communication, coordination, and collaboration skills, including the ability to challenge stakeholders.
  • Excellent legal, financial, and/or technical writing skills.
  • Thorough understanding of regulated clinical trials, drug development, GCP/ICH, and applicable regulatory guidelines.

Nice to have

  • Experience in a pharmaceutical or CRO environment.

Culture & Benefits

  • Full-time employment.
  • Potential incentive plans, bonuses, health and welfare benefits, and other benefits may be offered depending on the position.
  • Work within a global clinical research and healthcare intelligence organization.

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