Clinical Research Coordinator

vor 1 Woche

Lausanne, Schweiz Aktiia Vollzeit

Oversee several clinical studies ongoing at CHUV hospital
- Maintain expertise and understanding of clinical trial documentation, requirements and operational procedures for all these studies ongoing at CHUV hospital
- Control, and correct when required, study procedures at site to ensure these clinical trials are conducted in accordance with the study documentation and correct standard operations and procedures
- Participate to the monitoring visits together with the CRO and help resolve queries
- Be the referent of the studies for the clinical staff on site
- Provide technical help to resolve any issues with study materials
- Report inclusions rate and any study deviations to Clinical Operations Manager
- Be very dynamic, reactive and able to resolve any issues faced by the site staff
- Be proactive and autonomous
- Help the Clinical Project Manager to update clinical documentation for these studies
- Take part in administrative tasks such as updating Excel spreadsheet and document scanning

**Requirements**:

- Bachelor’s degree in clinical research, biology, or related disciplines, or laboratory technician
- Previous experiences at hospital and clinical research environment preferred
- Completed GCP training preferred
- Ability to problem-solve is required
- Ability to learn quickly is required
- Understand and speak English
- Very good communication skills
- Job located in Switzerland - Lausanne

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