6 дней назад
Innovative Medicine Site Contract Manager (Clinical Trials)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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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