Research Associate

Ref 2588921 | Date: 3 Nov 2026

Research Associate (ARC)

Company Description
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Swiss Visio Network is a network of ophthalmology centers at the forefront of medical techniques treating all ocular pathologies. Our teams guarantee personalized, top-quality care to patients, placing them at the center of attention. Swiss Visio distinguishes itself through its pleasant working environment and entrepreneurial spirit. The network currently includes 22 centers in French-speaking Switzerland, 3 in German-speaking Switzerland, and 1 in Ticino, and continues its expansion across the Swiss territory.

Job Description
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In order to strengthen its Research Center, Swiss Visio is looking for a motivated, rigorous, and autonomous Clinical Research Associate to participate in the development and coordination of its scientific activities.

• Your mission

Reporting to the Medical Management of the Swiss Visio Research Center, you will ensure the coordination and monitoring of clinical studies as well as the development of the center's research projects. You will collaborate closely with investigators, clinical teams, sponsors, and academic partners to guarantee the quality and compliance of the projects.

Your main responsibilities

• Implement, coordinate, and monitor clinical studies.
• Ensure compliance with regulatory, ethical, and scientific requirements (ICH-GCP).
• Prepare submissions to Ethics Committees and manage study documentation.
• Participate in monitoring visits, audits, and inspections.
• Control the quality and traceability of clinical data.
• Contribute to the drafting of protocols, publications, and scientific communications.
• Ensure the follow-up of research projects and academic collaborations.
• Participate in the development of partnerships and the search for funding.
• Ensure the administrative follow-up of research projects.

Qualifications
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• University education in the field of health, biomedical sciences, or equivalent.
• Proven experience in clinical research, ideally in multicenter studies.
• Good knowledge of the Swiss regulatory framework and ICH-GCP standards.
• Experience in the follow-up of clinical and multicenter studies CRA.
• Excellent writing, organizational, and interpersonal skills.
• Ability to manage several projects simultaneously with autonomy and rigor.
• Mastery of French and good command of English. German is an asset.

Additional Information
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• The opportunity to join a network of ophthalmology centers at the forefront of medical techniques.
• A motivating activity in a pleasant working environment.
• A corporate culture focused on excellence and the quality of human relations.

We pay great attention to the diversity of the life paths of our employees. Our positions are open to both women and men.

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