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9 дней назад

Senior Manager, Legal Council (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
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, Legal Council (Clinical Research): Providing operational support and guidance for clinical trial contracting across IQVIA Biotech with an accent on contract templates, legal alignment, and country-specific requirements. Focus on resolving complex contracting issues, maintaining global site contract libraries, and standardizing compliant processes across international site contracting teams.

Location: London, United Kingdom

Company

IQVIA 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, site contracting stakeholders, and global template developers.
  • Serve as the operational contact for complex contracting issues and coordinate timely resolution with internal Legal teams.
  • Advise stakeholders on approved contract positions, templates, policies, and escalation procedures.
  • Own and maintain the Global Site Contracts Library, including country-specific templates and guidance materials.
  • Lead contract template development, validation, translation coordination, version control, and continuous improvement.
  • Deliver training and support standardization, operational excellence, and compliance across site contracting activities.

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.
  • 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

  • Exposure to pharmaceutical and/or CRO environments.

Culture & Benefits

  • Full-time employment within a global clinical research and healthcare intelligence organization.
  • Cross-functional collaboration across complex international projects and site contracting teams.
  • Opportunity to contribute to the evolution of contracting processes and tools.

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