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5 years of work experience in clinical trials/pharmaceuticals company
Translation/Proofreading experience - Medical Device Manual(Patient monitor, Device adapter, etc.) - Clinical Trial Protocol - Informed Consent Form - Protocol Amendment Table of changes - Informed Consent Form Table of changes - Patient Reported Outcome, Patient Questionnaire - Patient Recruitment Material - Patient Card/Brochure - Lab Manual and Collection Flow Chart - Serious Adverse Event table - IRB submission/approval letters - Web site: Biopharmaceutical company - American health care system summary and FAQ - Post-Cognitive Debriefing Review for Patient Questionnaire - Language assessment test guidance - General MTPE - Business email