Non-clinical Scientific Writer Role:
-In this role, you will support the preparation and delivery of nonclinical regulatory documentation for global health authority submissions
- Working as part of a specialist scientific writing function, you will ensure documents are clear, scientifically robust, compliant and submitted in line with regulatory expectations.
- You will partner with nonclinical scientists, project leaders and regulatory colleagues to develop high-quality submission documents, study reports and supporting scientific materials.
- You will also contribute to process improvements, document standards and initiatives aimed at enhancing the efficiency and quality of regulatory documentation across the organisation.
- This is an excellent opportunity to work within a highly collaborative research and development environment supporting innovative medicines from early development through to marketing applications.
Your Background:
- Degree qualified in a Life Sciences discipline.
- Proven experience writing and editing scientific or regulatory documentation within a nonclinical environment.
- Knowledge of regulatory submissions and associated documentation requirements.
- Experience working with document management and scientific writing software.