Freelance Regulatory Writer
6 days ago
**The Company:**
An international consultancy with offices in the UK, US and across Europe, recently became part of a large group of companies with a global outreach. Focused on providing highly specialised Medical Writing services to Pharmaceutical, Biotech and MedicalDevice clients.
**Freelance Regulatory Writer Role:**
- Prepare clinical and regulatory documents including, but limited to, Clinical Study Protocols, Investigator’s Brochures (IBs), Clinical Study Reports (CSRs), Integrated Safety and Efficacy Summaries, Subject Consent Forms, Regulatory Submission (NDAs, BLAs,INDs, IMPDs etc.) and Briefing Documents.
- 100% remote working available.
- Outside IR35.
- 6-12 month contract length.
- Immediate start.
**Freelance Regulatory Writer Requirements**:
- 5 years+ of industry regulatory writing experience required
- Experience independently preparing a broad range of end-to-end clinical and regulatory documents.
- MSc or PhD in scientific, medical, clinical discipline preferred.
If this role isn't what you're looking for don't worry. At X4 Communications we cover all permanent and contract positions, with specialist industry sector teams. You can check out all of our roles on our website and sign up for job alerts so you're thefirst to know about a new opportunity.
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