Clinical Site Manager

Contract Details:

• Start Date: 01.12.2025
• Duration: Unlimited /…

Contract Details:

• Start Date: 01.12.2025
• Duration: Unlimited / open-ended
• Workload: 80-100%
• Location: Rotkreuz, Switzerland
• Home Office: Up to 40%

Role Overview:

We are looking for a Clinical Site Manager / Clinical Research Associate to coordinate, monitor, and manage in vitro diagnostic clinical studies across Europe. This position ensures studies are conducted according to protocol, regulatory requirements, and quality standards, contributing to product validation and regulatory submissions.

Key Responsibilities:

• Manage all aspects of clinical studies, including site selection, initiation, monitoring, and closeout
• Ensure compliance with study protocols, SOPs, GCP, ICH guidelines, and internal policies
• Liaise with study investigators, laboratories, and key opinion leaders
• Support data collection for regulatory submissions and product validation
• Collaborate with cross-functional teams to support post-launch activities

Qualifications / Must Haves:

• Bachelor's degree (Master's/PhD welcome) in Medical Technology, Science, or a relevant field
• Minimum 2 years of experience in clinical or laboratory research
• Knowledge of GCP, ICH guidelines, and clinical research regulations
• Excellent English communication skills (oral and written)
• Strong planning, organizational, and problem-solving abilities
• Ability to work independently and travel within Europe (25-30%)

Nice to Have:

• Experience in pathology or IVD studies

Why Join:

• Work in a high-impact clinical research environment
• Collaborate with top professionals and key opinion leaders in diagnostics
• Contribute to innovative solutions that improve patient care