Professional background
Medical doctor with extensive experience in clinical research, supporting sponsors, CROs, and study teams with practical, senior-level involvement across clinical trial operations and regulatory activities.
- Clinical Research Associate since 2007
- Medical background with clinical experience
- Direct support across operations and regulatory activities
- Freelance collaboration model with senior-level involvement
Clinical research scope
Professional experience includes support for clinical research in pharmaceuticals, medical devices, combination products, and in vitro diagnostic or companion diagnostic environments.
Support may include pre-market and post-market clinical activities, including selected real-world data or real-world evidence-related work where applicable.
Experience covers a broad range of therapeutic areas, including oncology, cardiology, neurology, ophthalmology, gynecology, internal medicine, rheumatology, pain management, and medical devices.
International experience
Professional experience includes collaboration with sponsors and CROs across Europe, North America, and China, including the USA, Canada, the UK, Belgium, the Netherlands, France, Spain, Italy, Poland, the Czech Republic, Hungary, Romania, Estonia, and China.
How I work
- Direct communication
- Senior-level involvement
- Flexible freelance collaboration
- Practical support across operations and regulatory activities
- Focus on efficiency, clarity, and compliant execution
Discuss your project
Please use the contact form if you need CRA, Study Startup, Regulatory Affairs, or Ethics Committee support in Germany.