Freelance Regulatory Writer

Description:

Are you currently looking for a new freelance position? Then look no further!

I am partnered with a global Biotech who are actively seeking multiple freelance medical writers to work on a number of their projects. This would be on a 6-12 month contract.

You will be preparing, developing and finalizing a number of regulatory documents for submission, including:

• CSR's
• IB's
• Briefing Documents
• CTD's
• Summaries
• Patient narratives
• SOPs

Requirements:

• Extensive clinical/scientific writing skills
• Scientific background - experience writing multiple clinical documents e.g. CSR's, study protocols, CTD documents
• Understanding of clinical research
• Fluent in written and spoken English
• 0.4 FTE+
• Remote (Within the EU)
• Flexible rate and start date