In this role, you will manage and oversee clinical trial activities across all study phases within Switzerland, ensuring high-quality execution and regulatory compliance. You will play a key role in site management, monitoring, and coordination between stakeholders. The position requires a strong operational mindset and the ability to drive studies efficiently from initiation through close-out.
Start Date: 01.06.2026
Duration: Permanent Position
Place of Work: Neuchâtel
Key Responsibilities
* Support the planning, coordination, and execution of clinical trials throughout all phases of the study lifecycle
* Contribute to feasibility assessments, site identification, and start-up activities including regulatory and ethics submissions
* Conduct on-site monitoring visits such as site initiation, routine monitoring, and close-out visits
* Ensure that clinical trials are conducted in compliance with study protocols, ICH-GCP guidelines, and applicable regulations
* Review and verify clinical data, source documents, and study records to ensure accuracy and completeness
* Prepare and maintain essential clinical documentation including monitoring reports and study-related correspondence
* Build and maintain strong relationships with investigational sites and external stakeholders
* Identify, track, and follow up on study-related issues, deviations, and corrective actions
* Coordinate site activities and support operational aspects of site management, including contracts and timelines
* Act as a key liaison between study sites, sponsors, and internal teams
* Support the preparation and submission of regulatory documentation and study updates where required
* Contribute to process improvements and ensure efficient study execution
Candidate Profile
* Degree in Life Sciences, Pharmacy, or a related discipline
* Extensive experience in clinical research, including several years in a CRA or similar role
* Strong knowledge of ICH-GCP and applicable clinical trial regulations
* Familiarity with the Swiss clinical research environment and site landscape
* Experience in monitoring clinical trials across multiple phases
* Strong documentation skills with attention to detail and quality standards
* Ability to manage multiple priorities and work independently
* Excellent communication and stakeholder management skills
* Fluent in English, French, and German
Job ID 18870
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