In this role you will be working on and looking over projects focusing on:
- Support the clinical medical writing team, in developing content for, writing and editing a variety of scientific and medical documents, including clinical protocols, informed consents (ICFs), clinical study reports (CSRs), investigator brochures (IBs), patient narratives and annual reports.
- Draft and manage documents that are well-organised, accurate, consistent, and in compliance with applicable company SOPs and regulations.
- Partner with Quality Assurance (QA) during audit of clinical documents to ensure timely response to findings.
- Ensures all clinical documents are standardised with the use of document templates, in order to ensure the quality and consistency of documentation across programs.
- 12 Months
- 0.5 FTE - 1.0 FTE
- Outside IR35
The ideal candidate will have a minimum of 5 years of work experience in the regulatory medical writing field and have experience either working directly with pharma, biotech or CRO's
The client is willing to be flexible on start date for the right candidate. However, interviews have occurred this week!!!
If this position sounds of interest, please do not hesitate to click on the appropriate links to apply or get in touch directly at