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6 дней назад

Innovative Medicine Site Contract Manager (Clinical Trials)

Формат работы
hybrid
Тип работы
fulltime
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
Innovative Medicine Site Contract Manager (Clinical Trials) (Clinical Trials/Contracting): Preparing, negotiating, and finalizing clinical trial agreements, ancillary documents, site budgets, and amendments with an accent on investigator-site contracting, fair-market-value budgets, compliance, and contract lifecycle management. Focus on resolving contractual and budget risks, tracking legal documents and metrics, supporting audits, and improving clinical trial site initiation efficiency.

Location: Seoul, South Korea; hybrid work format. Travel requirement: 10%.

Company

Johnson & Johnson MedTech develops healthcare solutions and innovative medicines aimed at preventing, treating, and curing complex diseases.

What you will do

  • Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company-sponsored and investigator-initiated studies.
  • Support the development of site and investigator budgets aligned with fair market value.
  • Manage contract amendments, legal document tracking, metrics, and site payment activities.
  • Assess contractual and budget risks with global CCS partners and escalate issues when appropriate.
  • Support clinical operations, audits, quality assurance requests, and compliance with study cost guidelines.
  • Recommend process improvements that reduce cycle time, create savings, and improve clinical trial site initiation efficiency.

Requirements

  • Bachelor’s degree in a relevant scientific or business discipline.
  • Experience in the pharmaceutical industry or clinical research, including at least two years of negotiation and contract experience.
  • Working knowledge of clinical development and clinical research processes.
  • Strong negotiation, problem-resolution, interpersonal, analytical, and workload-management skills.
  • Ability to work independently and effectively in cross-functional and virtual teams.
  • Fluency in English is required. Working knowledge of Microsoft Office and database management is also required.

Nice to have

  • Familiarity with healthcare compliance guidance such as HIPAA, FCPA, and Safe Harbor.
  • Previous experience working in virtual teams.
  • AI literacy and an AI-enabled mindset for responsible use of AI tools in daily work.

Culture & Benefits

  • Inclusive work environment focused on diversity, dignity, and individual contribution.
  • Collaboration with clinical investigator sites, clinical research organizations, commercial suppliers, legal, risk, quality, and other internal partners.
  • Regular work with global CCS teams.
  • Hybrid work arrangement with approximately 10% travel.

Hiring process

  • Submit a free-form resume and cover letter in English.
  • Applications remain open until the position is filled; only candidates passing resume screening will be contacted individually.

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