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12 дней назад

Global Site Contract Manager (Clinical Research)

86 500 - 216 000$
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
Global Site Contract Manager (Clinical Research): Managing contract strategy and start-up contracting activities for complex clinical studies and multi-protocol programs with an accent on investigator grant estimates, site agreements, regulatory compliance, and cross-country coordination. Focus on developing contracting systems and templates, analyzing contracting intelligence, maintaining project timelines and financial goals, and mentoring colleagues.

Location: Durham, North Carolina, United States of America

Base pay: $86,500.00–$216,000.00 annualized

Company

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

What you will do

  • Manage contract strategy and start-up contracting activities for selected sponsors, complex studies, and multi-protocol programs.
  • Develop investigator grant estimates, contracting strategies, contract and budget templates, systems, tools, processes, and training materials.
  • Coordinate with sponsors, study stakeholders, regions, and countries to deliver project scope in compliance with sponsor requirements and management plans.
  • Provide legal, operational, and financial contracting support for site agreements and complex clinical trials.
  • Analyze contracting intelligence, report performance metrics, and maintain project timelines, plans, databases, and CTMS records.
  • Mentor colleagues, provide technical guidance, deliver presentations, and support long-term client relationships.

Requirements

  • Bachelor's degree.
  • 5 years of relevant sponsor or clinical research organization clinical site contracting experience.
  • Demonstrable experience acting as an international contract expert.
  • Ability to support complex clinical trials while complying with regulatory requirements and local laws.
  • Experience collaborating with sponsors, stakeholders, study teams, and international regions and countries.

Culture & Benefits

  • Full-time employment.
  • Potential incentive plans, bonuses, and additional compensation may be available depending on the position.
  • Health and welfare benefits may be provided.
  • Equal opportunity employment environment.

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