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Member since Jan '20
Working languages:
Spanish to English English to Spanish English (monolingual) Spanish (monolingual)
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Dec 3, 2020 (posted viaProZ.com): Currently doing an English into Spanish translation of a 11,063-word Epilepsy webinar for the International League Against Epilepsy via TWB....more, + 9 other entries »
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Services
Terminology management, Translation, Editing/proofreading, AI + Human review (MT post-editing), Linguistic validation
Expertise
Specializes in:
Medical: Pharmaceuticals
Medical (general)
Medical: Oncology
Medical: Cardiology
Medical: Instruments
Medical: Health Care
Genetics
Medical: Dentistry
Nutrition
Rates
General rate: 0.17 USD per word / 110 USD per hour
Rates per language pair: Spanish to English - Standard rate: 0.17 USD per word / 110 USD per hour English to Spanish - Standard rate: 0.17 USD per word / 110 USD per hour English - Standard rate: 0.10 USD per word / 100 USD per hour Spanish - Standard rate: 0.10 USD per word / 100 USD per hour
English to Spanish: Clinical Trial Protocol Excerpt (English to Spanish) General field: Medical Detailed field: Medical: Pharmaceuticals
Source text - English This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled study designed to assess the efficacy and safety of the investigational product administered subcutaneously every four weeks.
The primary endpoint is the change from baseline in the Disease Activity Score (DAS28) at Week 24. Secondary endpoints include the proportion of subjects achieving ACR20, ACR50 and ACR70 responses, and changes in patient-reported outcomes.
Inclusion criteria include adult subjects aged 18 to 75 years with a confirmed diagnosis of the target condition for at least six months and inadequate response to at least one prior conventional therapy. Subjects with active infection, significant cardiovascular disease, or known hypersensitivity to the study drug will be excluded.
Translation - Spanish Este es un estudio de fase III, multicéntrico, aleatorizado, doble ciego y controlado con placebo, diseñado para evaluar la eficacia y la seguridad del producto en investigación, administrado por vía subcutánea cada cuatro semanas.
El criterio de evaluación principal es el cambio con respecto al valor inicial en el Índice de Actividad de la Enfermedad (DAS28) en la semana 24. Los criterios de evaluación secundarios incluyen la proporción de sujetos que alcanzan respuestas ACR20, ACR50 y ACR70, así como los cambios en los resultados reportados por los pacientes.
Los criterios de inclusión incluyen sujetos adultos de entre 18 y 75 años con un diagnóstico confirmado de la enfermedad objetivo durante al menos seis meses y una respuesta inadecuada a al menos un tratamiento convencional previo. Se excluirán los casos con infección activa, enfermedad cardiovascular importante o hipersensibilidad conocida al fármaco en estudio.
English to Spanish: Informed Consent Form (ICF) Excerpt (English to Spanish) General field: Medical Detailed field: Medical: Pharmaceuticals
Source text - English You are being invited to take part in a clinical research study. The purpose of this study is to evaluate the safety and efficacy of an investigational drug in adult patients with moderate to severe rheumatoid arthritis who have had an inadequate response to previous treatment.
If you agree to participate, you will be asked to attend scheduled visits at the study site, undergo blood tests and physical examinations, and complete questionnaires about your symptoms. Participation is voluntary and you may withdraw at any time without affecting your regular medical care.
Possible risks include injection-site reactions, headache, and upper respiratory tract infections. Your personal data will be treated confidentially and in accordance with applicable data protection regulations.
Translation - Spanish Se le invita a participar en un estudio de investigación clínica. El objetivo de este estudio es evaluar la seguridad y la eficacia de un medicamento en investigación en pacientes adultos con artritis reumatoide moderada a grave que no hayan respondido adecuadamente a tratamientos anteriores.
Si acepta participar, se le pedirá que acuda a las visitas programadas en el centro del estudio, que se someta a análisis de sangre y exámenes físicos, y que complete cuestionarios sobre sus síntomas. La participación es voluntaria y puede retirarse en cualquier momento sin que ello afecte su atención médica habitual.
Los posibles riesgos incluyen reacciones en el sitio de la inyección, dolor de cabeza e infecciones del tracto respiratorio superior. Sus datos personales se tratarán de manera confidencial y de acuerdo con las normas de protección de datos aplicables.
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Bio
Licensed physician and English↔Spanish medical translator with over 10 years of experience delivering accurate, culturally adapted translations for healthcare, pharmaceuticals, and clinical research. Delivered over 2.5 million words, including 905,865 words for Lexxika and 760,258 words for PPD/Thermo Fisher Scientific. Now combining owned DeepL Pro with Trados Studio 2021 and client-provided memoQ for hybrid physician-reviewed translations that deliver 2–3× faster turnaround while maintaining full MD-level accuracy and ICH-GCP/HIPAA compliance. Specialized in Clinical Trials, Regulatory Documentation (SmPC, SUSAR, DSUR, CTD), Medical Devices, Patient Information Leaflets, Informed Consent Forms, and therapeutic areas including Cardiology, Oncology, Infectious Diseases, Neurology, and Pneumology. Available immediately for new projects. Updated CV available upon request.
This user has earned KudoZ points by helping other translators with PRO-level terms. Click point total(s) to see term translations provided.
This user has reported completing projects in the following job categories, language pairs, and fields.
Project History Summary
Total projects
5
With client feedback
0
Corroborated
0
0 positive (0 entries)
positive
0
neutral
0
negative
0
Job type
Translation
4
Editing/proofreading
1
Language pairs
English to Spanish
5
Specialty fields
Other fields
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