I worked for 10 yrs. (2003-13) at the Reg. Affairs and QA Dept. of J&J Medical Italy, where I gained extensive knowledge on MDs, QMS, and pharmacovigilance. I was involved in the In-country Review of MD IFUs and labels translated by external agencies, and I provided EN>IT translations of FSNs and FSCAs. This experience allowed me to acquire a regulatory mindset. My EN>IT translation of a book on bariatrics is pending publication. Since 05/13, I’ve been translating CT-related documents.

» health and well being campaigns
» health-related benefits and diet programs
» health insurance plan information
» end-of-life videos for patients and families
» data sheets on chemicals and health exposure
» application and use medication and cosmeceuticals
» reports on pharma studies
» toxicity reports on animal studies
» articles for medical journals
» user manual for small procedures and clinical analyses
» personal documents, including patient's records and death certificates

Medical/scientific documentation (scientific articles, lab reports, lab manuals, etc.)
Devices, Pharmaceuticals, Surveys and Clinical Trials, Informed Consent Forms, Clinical Trials Agreements and Letters, Adverse Event Summaries, Medical Device Information, Lab Reports, Tender documents: Drugs and Drug sundries, Category B Clearance for Operational Unit of Nuclear Medicine: requests for clearance or updates to modifications on activities of Nuclear Medicine, etc.

Experience and Work History Since 1996: ◆ full-time freelance certified translator
I am registered as a Professional Translator at the Chamber of Commerce of Padua (Italy).
I am an Arabic-native freelance Translator based in Italy. Also I provide simultaneous and consecutive interpreting
Specialized in Finance, technical, pharmaceutical , and marketing texts.
I have worked for many companies over 1,000,000 words
I have a degree in Italian and translation
Sdl 2019, MemoQ

I deal mainly with the translation and linguistic validation of Clinical Outcomes Assessments (COAs) and Patient Reported Outcome (PRO) questionnaires, acting as language validation coordinator for Italy.

My work includes also ranslation and proofreading of ICFs, user manuals of medical equipment and surgical instruments and the adaptation to QRD templates, translation and readability user tests of PILs and SmPCs.

I have an MS in chemistry and am currently a PhD candidate at Columbia University working in the field of chemical biology. I have worked on outsourced translations from Menarini, Patheon and Teva, and have also done work for Gruppo Italiano di Trapianto di Midollo Osseo (GITMO), Agenzia Locale della Provincia di Bari (ASLBA) and L'Agenzia Italiana del Farmaco (AIFA). I have also translated reports and studies on various drugs and therapies by other research/medical entities.

Large experience in clinical protocols and medical literature of all kinds.

An in-house patent translation reviser until 2019, I regularly translate life sciences patents, but also marketing and training materials, general medical documentation, and questionnaires for patients and healthcare providers.

I treat each project with the greatest care. My goal is to deliver high-quality, well researched translations that help pharmaceutical companies effectively communicate their message to patients and professionals.

Interested? Contact me at [email protected]!

I hold an Italian Master in Medical amd Pharmacological Translation and I am familiar with a wide range of documents, such as SPCs, clinical trials, articles and research, drug patents, patient information leaflets, personal records and legal documents (informed consent...).
I am also familiar with medical devices (user manuals both for patients and surgeons).

Chemical engineer and industrial hygienist, I have the background for the research, production, and testing sectors of this field.
I regularly translate clinical records, clinical trial protocols, drug safety reports, process validation reports, deviation reports, informed consent forms, ethics committee minutes, material safety data sheets, etc.

Mainly worked for translation agencies, expert in pharma patents.

I have 8+ years of experience translating various types of pharmaceutical documents, including summaries of product characteristics (SmPC), informed consent forms for clinical trials on investigational medicinal products, various patient-facing materials (dosing instructions, package leaflets, etc.), I also have extensive experience translating medical journal articles about pharmaceutical products in a post-marketing context. Nearly all of my pharma work has come through LSPs.

Medical and veterinary articles
Clinical trial protocols and informed consent forms for patients
Description of medical and pharmaceutical products
Specialised webpages
Case reports, disease cards
Prevention, diagnosis and treatment guides
Labels, inserts
Presentations for conferences

I am a native English speaker, and I have been a full-time freelance translator since 2009. I have hundreds of thousands of words of experience just with pharmaceutical and clinical trials. Most of my work is legal, financial, and marketing texts, which makes me a suitable translator also for Ethics Board minutes, training materials, and other projects in the sector.

Clinical trials
eCTD (modules 2 and 3)
SPC and IPLs
Occasionally: Research articles and marketing material

I have been providing brief translations (written and via site translation) of various medications to clients, when interpreting for a number of different medical practitioners. I worked for the now Cancer Council, in Melbourne, in research and medical trials as a bilingual telephone consultant. Currently I am also a personal assistant to a psychiatrist, and handle all related information contained in the medical reports, including details of medications and prescriptions.

I have translated clinical trial protocols and related regulatory materials; patient records; adverse event reports; journal articles; marketing brochures, and more. I also do revision and editorial work, proofing and back translation, primarily for leading agencies.
More than 30 years experience in clinical medicine, now retired from clinical work; PhD in History of Medicine; writer; author of several publications including a 2016 textbook on medical innovations.

Linguistically Validated Translation Expert Reviewer (reconciliation, harmonization, back-translation)
Drug registration dossiers, EMA, SPCs, PILs, labeling, etc.
Clinical trials (Study Protocol, ICFs, PROs, etc.)
Ultra-specialized topics as bio-medicine, bio-research, gene therapy, molecular lab, oncology, etc.

In my 10-years experience as a project manager I have managed hundreds of projects for top pharmaceutical companies, learning to speak their language.
In 2017 I started my freelance career specializing in the medical and pharmaceutical fields.
Among the documents I usually translate in this field: Patient information leaflets, Clinical and pre-clinical trials, reports and protocols, market research documents, Brochures and press releases
I also work in the medical devices and dentistry fields

Medical studies in Italy first and then in Germany until MD graduation. Internship in Internal Medicine, Radiology and Surgery.

Translation, Proofreading, SME validation

– Physician/Patient facing
– Clinical Trials, ICF
– SPC and PIL
– Orphan Drugs
– Expert reports, clinical reports, case history
– Questionnaires
– Clinical Chemistry
– Microbiology
– Molecular Medicine
– NCCN Guidelines® in Oncology
– Advanced training modules for Medical Specialists accr. EACCME®

➸Clinical trial protocols, IBs, ICFs, SmPCs, PILs according to the most recent EMA templates, "Dear Doctor" letters, medical equipment & lab instrument IFUs, marketing brochures. Preferred therapeutic areas include: oncology, gynaecology, food-related diseases.
➸I mainly work for leading translation agencies and CROs, the names of which I cannot disclose due to NDAs. Strict confidentiality assured.
Prices include review by a second pharma expert for highest accuracy and quality.

PhD in veterinary medicine, experience in clinical research, diploma in general translations, and in screen translations. I have translated materials such as: Informed Consents; Clinical Trial Protocols; Guidelines; Product Brochures & Fact-Sheets; Medical & Scientific Reports; User Manuals of Medical Instrumentation and Equipment; Safety Sheets of Drugs and Chemical Substances; Technical Specifications; Assurance & Quality Control Certifications, Marketing
Authorizations.

I worked as a sales representative for 2 pharmaceutical companies before starting a career as a freelance translator, 12 years ago.
I mainly deal with summaries of product characteristics, product leaflets and various documents concerning marketing authorisation applications. I also work on clinical trial agreements, physician surveys, sales aids and all kinds of pharmaceutical and medical (both human and veterinary) texts.
My clients generally are translation agencies.

I am specialized in the translation of marketing-related texts and catalogues for medical devices. I have also translated clinical trials, especially in psychiatry. I also have an interest in psycology and psychotherapy.

I am an italian native patent translator experienced in the pharmaceutical and biotech field. My CAT tool is Studio 2015