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3 дня назад

Contract Negotiator (Clinical Trials)

Формат работы
onsite
Тип работы
fulltime
Английский
c1
Страна
Netherlands
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Contract Negotiator (Clinical Trials): Developing and negotiating investigator grants, clinical trial agreements, contract language, and budget templates for clinical research projects in the Netherlands with an accent on sponsor collaboration, regulatory compliance, and contracting efficiency. Focus on managing site agreements, maintaining contracting systems, reporting performance metrics, and supporting study teams throughout trial initiation and maintenance.

Location: Amsterdam, Netherlands

Company

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

What you will do

  • Develop investigator grants, estimates, contracting strategies, proposal text, contract language, and budget templates.
  • Maintain contracting systems, tools, processes, and training materials for assigned sponsors, studies, and multi-protocol programs.
  • Collaborate with sponsors, stakeholders, and regional and country teams to deliver project scope in line with sponsor requirements and management plans.
  • Provide legal, operational, and financial contracting support for site agreements and clinical trial initiation and maintenance.
  • Monitor contracting efficiency, project timelines, financial goals, performance metrics, and out-of-scope activities.
  • Support quality management and mentor or coach colleagues through training and knowledge sharing.

Requirements

  • Bachelor’s degree in a related field, or two years of relevant sponsor or clinical research organization clinical site contracting experience.
  • Experience negotiating clinical trial agreements with sites in Belgium or the Netherlands.
  • Strong negotiation and communication skills, including the ability to challenge constructively.
  • Understanding of the regulated clinical trial environment, drug development processes, and clinical trial contract management.
  • Fluent English required.

Culture & Benefits

  • Work within an international clinical research and healthcare intelligence organization.
  • Collaborate with sponsors, study teams, stakeholders, and regional and country teams.
  • Contribute to quality standards, regulatory compliance, and efficient clinical trial delivery.

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