5 дней назад
Site Contract Manager - cFSP, Hungary (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Site Contract Manager - cFSP, Hungary (Clinical Research): Negotiating, preparing, and executing clinical trial site agreements and related legal documents with an accent on contract compliance, study start-up, budgets, and payment schedules. Focus on resolving contractual issues, coordinating sponsors and research sites, and keeping site activation timelines and financial milestones on track.
Location: Budapest, Hungary
Company
Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Negotiate clinical trial contracts with research sites and ensure timely completion in line with quality and compliance requirements.
- Manage contract amendments, additional agreements, contract terms, payment schedules, and budget templates.
- Support contract planning and study start-up activities for assigned sponsors, studies, and programs.
- Develop investigator grants, site budgets, contracting plans, and proposal documents.
- Coordinate with sponsors, legal teams, research sites, and regional study start-up stakeholders.
- Monitor contract milestones, timelines, and financial goals while providing operational and financial guidance to study teams.
Requirements
- Bachelor’s degree or equivalent.
- 3–5 years of experience in clinical research contract management or a similar role.
- Familiarity with clinical trial processes, regulatory requirements, and contract lifecycle management.
- Strong analytical, organizational, negotiation, and communication skills.
- Ability to work in Budapest, Hungary.
Culture & Benefits
- Work as an integrated member of a leading sponsor’s team through a Clinical Functional Service Partnership.
- Gain exposure to clinical research programs across development phases and therapeutic areas.
- Access global expertise, career development, and support from a large clinical research organization.
- Collaborate with pharmaceutical and biotechnology partners on studies supporting innovative treatments.
- Develop sponsor-facing expertise and opportunities for long-term growth in clinical research.
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