From Silicon Valley to Swiss Clinical Research
I have been a writer and editor of scientific, medical, and technical content for over 20 years. Based in Neuchâtel, Switzerland, my career has spanned across Europe and California, allowing me to build a truly global perspective on technical communication.
My journey began managing complex technical documentation for leading global technology firms. This foundational expertise in distilling complex systems led to a role in program planning and management at a major international public health agency in Geneva. For the past 12 years, I have focused my expertise exclusively within the medical and scientific writing sectors.
Specialized Regulatory & Scientific Expertise
I am an ICH-GCP (Good Clinical Practice) certified editor. Over a 10-year tenure as a Scientific Editor for a multinational corporation, I honed my ability to navigate high-stakes regulatory and publishing environments. My daily focus included coordinating the submission of clinical studies on www.clinicaltrials.gov, ensuring strict compliance with evolving registry requirements.
My broad experience also encompasses:
- Editing and submitting manuscripts to scientific journals, and collaborating with authors to respond to peer review comments.
- Providing rigorous editorial support for the production of clinical study protocols, clinical study reports, and investigator brochures.
- Creating Instructions For Use (IFU) for medical devices and managing content translation across multiple languages.
- Collaborating with study teams to write and maintain Standard Operating Procedures (SOP).
Whether you are preparing a pivotal manuscript for publication or navigating the administrative heavy lifting of clinical trial disclosure, I provide the meticulous attention to detail required to push your project across the finish line.
Contact Me About Your Project