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11 дней назад

Investigator Services Analyst (Clinical Trials)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
SK
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
Investigator Services Analyst (Clinical Trials): Supporting investigator site contracting and study start-up activities in Seoul with an accent on clinical trial agreements, site budgets, grant estimates, and regulatory compliance. Focus on drafting, reviewing, negotiating, and executing contracts, coordinating stakeholders, and maintaining accurate contracting data in CTMS and related systems.

Location: Seoul, Republic of Korea

Company

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

What you will do

  • Support start-up contracting activities for sponsors, studies, and multi-protocol programs, including pre-award work.
  • Develop investigator grant estimates, proposal text, contracting strategies, and supporting study documentation.
  • Draft, review, negotiate, and execute investigator site contracts and amendments.
  • Lead site budget development and negotiations with investigational sites.
  • Coordinate sponsors, stakeholders, and regional and country teams to deliver project scope and timelines.
  • Maintain contract systems, CTMS records, databases, tracking tools, project plans, and contracting performance metrics.

Requirements

  • Bachelor’s degree.
  • At least 2 years of site contracting experience, including Clinical Trial Agreement handling.
  • Experience with initial and amendment CTA drafting, review, negotiation, and execution.
  • Experience leading site budget development and negotiations.
  • Experience in life sciences, a medically related field, biopharmaceuticals, or clinical research.
  • Strong communication and stakeholder management skills.

Culture & Benefits

  • Work includes collaboration with sponsors, study stakeholders, and regional and country teams.
  • Responsibilities are governed by contract management, quality, regulatory, project, and financial standards.
  • The role supports the development and commercialization of medical treatments and improved patient outcomes.

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