Working languages:
English to French

Nadia A.
EN>FR clinical trial translations

Morocco

Native in: French Native in French
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10 positive reviews

0.0 (10 reviews)


User message
Medical translations that change lives
Account type Freelance translator and/or interpreter, Identity Verified Verified member
Data security Created by Evelio Clavel-Rosales This person has a SecurePRO™ card. Because this person is not a ProZ.com Plus subscriber, to view his or her SecurePRO™ card you must be a ProZ.com Business member or Plus subscriber.
Affiliations This person is not affiliated with any business or Blue Board record at ProZ.com.
Services Translation, Editing/proofreading, AI + Human review (MT post-editing) , Website localization, Software localization
Expertise
Specializes in:
Medical: InstrumentsMedical: Pharmaceuticals
Biology (-tech,-chem,micro-)Medical (general)
Medical: Health CareMedical: Cardiology
Medical: DentistryChemistry; Chem Sci/Eng
PatentsIT (Information Technology)

KudoZ activity (PRO) PRO-level points: 501, Questions answered: 298
Payment methods accepted Wire transfer
Experience Years of experience: 15. Registered at ProZ.com: Feb 2016. Became a member: Aug 2016.
Credentials English to French (SDL)
Memberships N/A
Software Across, Adobe Acrobat, Adobe Illustrator, Adobe Photoshop, CafeTran Espresso, Catalyst, Crowdin, Indesign, MateCat, memoQ, MemSource Cloud, Microsoft 365, Microsoft Excel, Microsoft Word, Passolo, Plunet BusinessManager, Powerpoint, Protemos, SDLX, Smartcat, Smartling, Trados Studio, Transifex, Translation Workspace, Wordfast, XTM, XTRF Translation Management System
Professional practices
Bio
I am a medical translator at Translation For Life with 12+ years of experience, helping MedTech and pharmaceutical companies achieve compliance with the linguistic requirements of their product milestones. In doing this, I am also helping make life better for people with diseases, disabilities or simply unmet medical needs.

I worked as a freelance translator with hundreds of companies from around the world, including LSPs, CROs and MedTech/Pharmaceutical companies.

In my current role, I focus on micro-specialized, high-impact collaborations, which allow me to fine-tune my skills with unique learning opportunities, while also being proud and thankful for every single opportunity crossing my path that could contribute to someone's well-being and happiness.
This user has earned KudoZ points by helping other translators with PRO-level terms. Click point total(s) to see term translations provided.

Total pts earned: 531
PRO-level pts: 501


Language (PRO)
English to French501
Top general fields (PRO)
Tech/Engineering230
Medical162
Other36
Marketing26
Science24
Pts in 2 more flds >
Top specific fields (PRO)
Patents64
Medical: Instruments61
IT (Information Technology)51
Medical: Pharmaceuticals44
Chemistry; Chem Sci/Eng43
Medical (general)32
Mechanics / Mech Engineering31
Pts in 14 more flds >

See all points earned >
Keywords: Life Sciences Translation, Medical Localization, Back-Translation & Reconciliation, Linguistic Validation, Cognitive Debriefing, Translation Memory (TM) & Termbases (TB), Computer-Assisted Translation (CAT) Tools, Post-Editing Machine Translation (PEMT), Plain Language Summaries (PLS) / Layperson Summaries, Informed Consent Forms (ICF). See more.Life Sciences Translation, Medical Localization, Back-Translation & Reconciliation, Linguistic Validation, Cognitive Debriefing, Translation Memory (TM) & Termbases (TB), Computer-Assisted Translation (CAT) Tools, Post-Editing Machine Translation (PEMT), Plain Language Summaries (PLS) / Layperson Summaries, Informed Consent Forms (ICF), Clinical Trial Protocols & Amendments, Patient-Reported Outcomes (PRO / ePRO), Clinical Outcome Assessments (COA / eCOA), Investigator Brochures (IB), Case Report Forms (CRF / eCRF), Clinical Study Reports (CSR), Patient Diaries & Questionnaires, Adverse Event (AE) / Serious Adverse Event (SAE) Reports, Participant Recruitment Materials, Good Clinical Practice (GCP) / ICH-GCP Guidelines, FDA Regulations (US Food and Drug Administration), EMA Regulations (European Medicines Agency) / EU CTR (Clinical Trials Regulation), Informed Consent Process, Pharmacovigilance (PV) Translation, Standard Operating Procedures (SOPs), Pharmacology / Pharmacokinetics (PK) / Pharmacodynamics (PD), Oncology / Cardiology / Neurology (List your specific areas of expertise), Medical Device Documentation, In Vitro Diagnostics (IVD), Clinical Research Methodology. See less.


Profile last updated
Nov 7



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