Назад
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7 дней назад

Contract Negotiator (Clinical Research)

62 800 - 157 100$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
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 (Clinical Research): Developing global contracting strategies, agreements, budgets, and payment language for clinical studies with an accent on sponsor requirements, regulatory compliance, and contract efficiency. Focus on negotiating site agreements, coordinating cross-functional stakeholders, analyzing contracting metrics, and maintaining timelines and financial goals.

Location: United States; must be located within commuting distance of Dallas, Texas or Minneapolis, Minnesota

Salary: $62,800–$157,100 annual base pay

Company

IQVIA 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 language, contract language, payment language, and budget templates.
  • Manage contracting systems, tools, processes, tracking data, timelines, and project plans for clinical studies and multi-protocol programs.
  • Collaborate with sponsors, study teams, stakeholders, and regional and country teams to deliver contracting activities.
  • Provide legal, operational, and financial contracting support for site agreements and clinical trial initiation and maintenance.
  • Analyze and communicate contracting intelligence, performance metrics, timelines, and out-of-scope activities.
  • Support quality management, client presentations, colleague mentoring, and training delivery.

Requirements

  • Bachelor's degree in a related field or an equivalent combination of education, training, and experience.
  • At least 5 years of relevant sponsor or clinical research organization clinical site contracting experience, including global or regional contract negotiation.
  • Strong negotiation, communication, interpersonal, legal, financial, and technical writing skills.
  • Knowledge of regulated clinical trials, drug development, GCP/ICH guidelines, regulatory requirements, SOPs, and contract management.
  • Ability to work independently in a matrix environment, develop alternative contract terms and financial options, and manage project timelines.
  • Must be located within commuting distance of Dallas, Texas or Minneapolis, Minnesota.

Culture & Benefits

  • Full-time employment with health and welfare benefits.
  • Opportunity to work with global sponsors and cross-functional clinical research teams.
  • Responsibilities include mentoring colleagues and delivering training materials.
  • Additional incentive plans, bonuses, or other compensation may be available depending on the position.

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