Назад
Company hidden
4 дня назад

Associate Global Site Contracts Manager (Clinical Research) - Spain

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:
/
TL;DR
Associate Global Site Contracts Manager (Clinical Research) - Spain (clinical trials and contract negotiation): Developing global contracting strategies, investigator grants, budgets, and contract language for clinical trial site agreements with an accent on sponsor requirements, regulatory compliance, and financial objectives. Focus on negotiating regional and global contracts, coordinating study teams and stakeholders, maintaining CTMS and contracting systems, and improving delivery against project timelines.

Location: Madrid, 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 global contracting strategies, investigator grants, estimates, proposal text, contract language, payment language, and budget templates.
  • Support the start-up, initiation, and maintenance of clinical trials through site agreement contracting.
  • Coordinate with sponsors, study teams, stakeholders, and regional and country teams to deliver project scope.
  • Provide legal, operational, and financial contracting support while maintaining regulatory compliance.
  • Maintain CTMS, contracting systems, databases, tracking tools, timelines, and project plans.
  • Report contracting performance, support quality management, mentor colleagues, and present to clients.

Requirements

  • Bachelor's degree in a related field.
  • At least 5 years of relevant sponsor or clinical research organization experience in clinical site contracting.
  • Demonstrable global and/or regional experience as a contract negotiator.
  • Experience supporting clinical trial contracts, budgets, regulatory requirements, and project timelines.

Culture & Benefits

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

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →