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21 день назад

Contract Negotiator - FSP - Czech Republic (Clinical Trials)

Формат работы
onsite
Тип работы
fulltime
Английский
c1
Страна
CR
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
Contract Negotiator - FSP - Czech Republic (Clinical Trials): Developing investigator grants, contract language, budgets, and contracting strategies for clinical trial site agreements with an accent on negotiation, compliance, and financial accuracy. Focus on coordinating sponsors and study teams, managing contracting systems, and ensuring efficient contract delivery within project timelines.

Location: Prague, Czech Republic

Company

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

What you will do

  • Develop investigator grants, estimates, contracting strategies, and proposal text for clinical research projects.
  • Develop contract language and budget templates for site agreements.
  • Maintain contracting systems, tools, processes, and training materials according to project plans.
  • Coordinate with sponsors, study teams, stakeholders, and regional and country teams to deliver project scope.
  • Provide legal, operational, and financial contracting support for clinical trial initiation and maintenance.
  • Report contracting performance, support quality standards, and mentor colleagues when required.

Requirements

  • Bachelor's degree in a related field or two years of relevant sponsor or clinical research organization site-contracting experience.
  • Experience negotiating clinical trial agreements with sites in the Czech Republic.
  • Strong understanding of the regulated clinical trial environment and drug development process.
  • Good understanding of clinical trial contract management.
  • Strong negotiation and communication skills, including the ability to challenge proposals constructively.
  • Fluent English required.

Culture & Benefits

  • Full-time employment at a global clinical research and healthcare intelligence organization.
  • Work involves collaboration with international sponsors, stakeholders, and study teams.
  • Responsibilities are aligned with quality management, regulatory compliance, project timelines, and financial goals.

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