Study Administrator (Hybrid) – Luzern
syneoshealth · CHE-Client
Job description
About the role
Syneos Health is seeking a Study Administrator to support a single‑sponsor partnership in Switzerland. This hybrid position requires you to work 2‑3 days per week from our Luzern office, handling clinical documentation and site‑management activities.
Key responsibilities
- Prepare, distribute, archive, and manage clinical documents, including investigator folders both physically and electronically.
- Support the Clinical Monitoring Team with site‑management tasks, acting as sponsor liaison and ensuring protocol compliance.
- Maintain clinical tracking data in databases, process inbound/outbound regulatory documents, and coordinate material shipments.
- Assist with budget, contract, and payment management, including CTRAs negotiation and financial compliance monitoring.
Required profile
- Completed vocational training in administration or medical field (e.g., KV, MPA, FAGE).
- Strong interest in healthcare and clinical research with good organizational skills.
- Excellent German and English communication; French or Italian is a plus.
- Ability to handle multiple tasks in a fast‑changing environment.
Required skills
- Proficiency in MS Office.
- Experience with AI tools and automation technologies.
- Quick learner of new IT applications and system‑affinity.
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Published 48 minutes ago
Expires 1 month from now
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syneoshealth
CHE-Client
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