Job Description
Responsibilities
- Support the clinical operations team in managing trial documentation, site communication, and study supplies.
- Maintain and update trial information in CTMS and eTMF systems.
- Coordinate contracts, insurance certificates, and vendor-related activities.
- Assist with SOP reviews, team meetings, and cross-functional collaboration.
- Supporting in general documentations and administration
Qualifications and Experience
- Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required;
- Minimum 2 years of experience in clinical research – can have more, but not necessary.
- Strong organizational and communication skills in English.
- Proficient in MS Office and able to manage multiple priorities independently.
- Detail-oriented, team player, and results-driven.
Clinical Operations Coordinator • Basel and NW Switz...
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