Email                       [email protected]

Skype                      live:.cid.19027e31781958ff

You are already one step ahead!

I have worked with multinational translation companies and end clients. A service provider in the field I treat all sensitive information as confidential and take steps to protect that confidentiality. I ensure consistent delivery of work of a high professional standard and accept responsibility for the quality of work I deliver. No matter any unforeseen problems I may encounter, I always deliver meet agreed-upon terms.

If you want to work with me, please email me or leave me a message.

  Degree awarded: Bachelor of Science

          Specializing in:

• AI/IT/Software: Quality Evaluation and Improvement, multilingual content creation, language analysis, localization
• Technology/Computer: XML, HTML, and database files, marketing materials: Brochures, catalogues, and packaging, training materials, websites and apps, product specifications/user manuals, patents, technical reports, mobile apps/software applications, web content, , documentation
• Advertising/E-Commerce/Consumer goods/Video tutorials/Campaign
  : Websites and product information, branding materials and brochures, email campaigns, press releases, advertising campaigns, Ad copy for print and electronic publications, marketing campaigns, brochures, catalogues, and packaging, financial reports, product specification/user manuals, legal documents and policies
• Research: Protocols investigator, brochures, informed consent forms, adverse event reports, case source documents for endpoint adjudication
• Medical device: Operating, maintenance and installation manuals, instructions for use, regulatory compliance documents for European Union and Asian countries, software application interfaces and documentation, package inserts and labels, patents for medical and surgical devices, manufacturing process descriptions
• Science: Regulatory affairs, sales&marketing, registration dossiers, websites-professional/consumer, CMC documentation, software and hardware, labels and package inserts, promotional materials, instructions for use (IFUs), marketing collateral, case report forms (CRFs), manufacturing, site operations manuals, GMP documentation, institutional contracts, SOPs, IVRS prompts, batch records and MBRs, Serious adverse event (SAEs), pharmacovigilance, informed consent forms (ICFs), patient recruitment materials, patient reported outcomes (PROs), patient questionnaires, clinical research, patents, study protocols, scientific articles, IRB/ethics committee submissions, lab reports, clinical trial agreements (CTAs), validation reports, investigator brochures, eLearning, IND and NDA documentation, multimedia, sales training, declaration of conformity, patient education (CMI and PHI), adverse event report forms, deviation reports, postmarketing surveillance, data sheets, validation reports, QMS audit documentation, patient diaries