Expert Linguistic Validation and Clinical Research Support
I provide specialized medical and technical translation services for global LSPs and CROs, offering deep expertise in the high-stakes life sciences sector. My work focuses on the intersection of linguistic precision and regulatory compliance, supporting long-term projects through content migration, data reconciliation, and daily linguistic validation. I am highly experienced in the methodology of cognitive patient interviews, ensuring that clinical instruments are culturally relevant and conceptually equivalent across languages.
I am a dedicated specialist in the translation and review of Clinical Outcomes Assessments (COAs) and their electronic counterparts, including eCOA, PRO/ePRO, ClinRO, and ObsRO. My technical fluency extends to the core documentation required for global clinical trials and market authorization, including:
- Informed Consent Forms (ICF)
- Summaries of Product Characteristics (SmPC)
- Patient Information Leaflets (PIL)
With a workflow designed to meet the rigorous quality demands of industry leaders like RWS Life Science, Lionbridge, and ICON Clinical Research, I deliver accurate, submission-ready content that facilitates seamless global research and pharmaceutical development.
Other clients include Siemens Healthineers, GE HealthCare, Abbott Laboratories, Glaxosmithkline, Cepheid, St Jude, Crucell, Pfizer, AstraZeneca, Brainlab.


Why Work With Me?
I pride myself on being a highly flexible partner dedicated to delivering high-quality MTPE, translation, and editing services strictly on schedule. While my standard office hours are 09:00 to 18:00 CET, I understand the fast-paced nature of international projects; I frequently work evenings and weekends to ensure your deadlines are met across all time zones, from the USA to India and China.
My core approach:
- Proven Technical Expertise: I have an extensive background in reviewing complex scientific texts and a broad academic foundation in English, Geography, and Swedish Law.
- Reliable Communication: I believe clear communication is the key to a successful project; I make it a point to confirm all emails within the same business day so you are never left wondering about the status of your task.
- Software Versatility: I am fully equipped with my own licenses for SDL Studio 2024 and MemoQ 11, and I am highly proficient in industry-standard tools like XTM, Wordbee, InDesign, and Microsoft 365.
Whether it is a precise medical report or a complex legal contract, I bring years of technical experience and a “solutions-first” mindset to every text I handle.
During a six week period in 2024 I worked in-house in Forchheim, Germany at Siemens Healthineers. I tested several software packages for CT scanners, Swedish against the source in close cooperation with local staff and external specialists.

I work for Icon Clinical Research on a daily basis, validating medical questionnaires, reconciliations, translations, reviews, migrations, eCOA, cognitive interviews with patients, reviews in close cooperation with medical specialists.


I translate and review large volumes of technical, medical texts for GE HealthCare on a regular basis. Image left GE HealthCare’s Giraffe system for which I reviewed the IFU. Image right GE HealthCare’s CT-scanner wfor which I reviewed large volumes of content and the IFU. Both images created with Imagen.