I’m looking for a freelance regulatory writer who can support a medical device client of mine – it’s an initial 2 month project, likely around 20-25 hours per week with some flex. Main deliverables will be supporting with technical files, plans, preparing study reports and clinical evaluation reports. It’s a small company, at a really exciting stage of their growth so this could become a great long term gig for the right freelancer! Key requirement is experience in the medical device space.

Looking for a start in late April and running until mid June, with the potential for extension!