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23 часа назад

Senior Site Contracts Associate (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Brazil
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Senior Site Contracts Associate (Clinical Research): Developing global contracting strategies, site agreements, investigator grants, and budget templates for clinical trials with an accent on contract negotiation, regulatory compliance, and financial planning. Focus on creating alternative contract language, coordinating sponsors and study teams, and maintaining efficient contracting delivery across regional and global programs.

Location: São Paulo, Brazil

Company

IQVIA Biotech is a full-service contract research organization serving biotech sponsors with clinical research, healthcare intelligence, and life sciences services.

What you will do

  • Develop global contracting strategies, investigator grants, estimates, proposal text, contract language, payment terms, and budget templates.
  • Support start-up contracting activities for sponsors, clinical studies, and multi-protocol programs.
  • Maintain contracting systems, tools, processes, and training materials according to project plans and agreed strategies.
  • 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 site agreements and study initiation.
  • Track contracting performance, timelines, financial goals, quality standards, and out-of-scope activities while mentoring colleagues.

Requirements

  • Bachelor's degree in a related field.
  • 3–5 years of relevant clinical site contracting experience at a sponsor or contract research organization, including regional or global contract negotiation.
  • Strong negotiation, communication, legal, financial, and technical writing skills.
  • Understanding of regulated clinical trials, the drug development process, clinical trial contract management, and applicable regulatory requirements.
  • Ability to apply GCP/ICH guidelines, standard operating procedures, and corporate standards.
  • Ability to develop alternative contracting language, terms, and financial options.

Culture & Benefits

  • Work with biotech sponsors on clinical research programs intended to accelerate innovative medical treatments.
  • Collaborate across sponsors, study teams, regional teams, and country stakeholders.
  • Participate in quality management, knowledge sharing, and colleague mentoring.

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