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1 день назад

Site Contract Negotiator - Spain - Sponsor dedicated

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Spain
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Site Contract Negotiator - Spain - Sponsor dedicated (Clinical Research): Developing local contracting strategies, agreements, payment language, and budget templates for sponsor-dedicated clinical trials with an accent on investigator grants, site contracting, and regulatory compliance. Focus on negotiating contracts, supporting study teams with legal and financial expertise, and maintaining contracting efficiency across assigned studies.

Location: Barcelona, Spain

Company

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

What you will do

  • Develop local contracting strategies for selected sponsors, studies, and multi-protocol programs.
  • Prepare investigator grants, estimates, contract language, payment terms, budget templates, and proposal text.
  • Maintain contracting systems, tools, processes, and training materials in line with project plans and sponsor requirements.
  • Collaborate with sponsors, study stakeholders, and regional and country teams to deliver contracting activities.
  • Provide legal, operational, and financial contracting support to study teams for clinical trial site agreements.
  • Monitor contracting performance, timelines, financial goals, and out-of-scope activities.

Requirements

  • Bachelor's degree in a related field.
  • 3–5 years of clinical site contracting experience with a sponsor or clinical research organization, including global or regional contract negotiation experience.
  • Experience with investigator-initiated or collaborative studies.
  • Strong negotiation, communication, interpersonal, legal, financial, and technical writing skills.
  • Understanding of the regulated clinical trial environment, drug development process, and clinical trial contract management.
  • Ability to exercise independent judgment, challenge appropriately, and make calculated decisions.

Culture & Benefits

  • Work in a global healthcare intelligence and clinical research environment.
  • Collaborate with sponsors, study teams, and international regional and country stakeholders.
  • Participate in a culture focused on integrity, diversity, inclusion, belonging, and equal opportunity.

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