FSP Site Start Up Specialist
Thermo Fisher Scientific · Budapest, Hungary
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Thermo Fisher Scientific seeks a Site Start Up Specialist in Budapest to support clinical trial site activation and approval processes. The role involves coordinating with internal teams and external partners to manage essential documentation, track site readiness, and ensure timely study initiation across assigned sites.
What they're looking for
- Bachelor's degree or international equivalent
- 2+ years clinical research site start-up experience in pharma, CRO, or vendor
- Knowledge of FDA and ICH-GCP guidelines for clinical research
- Understanding of clinical trial agreements, budgeting, and fair market value principles
- Proficiency in Microsoft Excel, Word, and PowerPoint
- Strong organizational, decision-making, communication, and negotiation skills
What you'll be doing
- Collect, review, and ensure completion of site essential documents including ICF, FDF, 1572, and CVs
- Partner with internal Study Startup teams, CROs, and Clinical Operations to improve site start-up metrics
- Track communications and actions with sites to maintain study timelines and identify activation delays
- Maintain accuracy and completeness of electronic Trial Master Files for assigned sites during activation
- Escalate and support resolution of issues identified by CROs and Clinical Operations teams
Privacy & handoff
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