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We are currently looking to recruit a freelance medical writer with proven experience writing technical documentation including primarily clinical evaluation reports, and associated clinical and PMS documentation. Experience with other parts of the technical file as defined by annex II of EU MDR is a bonus. You must have an excellent command of the English language.ResponsibilitiesWriting technical documentation for clients of MedRAS to ensure compliance with EU, UK and other global medical device regulatory requirements. QualificationsAn academic qualification in a science, engineering or medical discipline is a strong desirable but is not mandatory. However you must have an excellent command of the English language.
