At a Glance
- Tasks: Author and edit regulatory documents while collaborating with diverse teams.
- Company: Leading Regulatory Affairs consultancy with a focus on innovation.
- Benefits: Fully remote role, flexible hours, and opportunities for professional growth.
- Other info: Join a dynamic team and enhance your career in a supportive environment.
- Why this job: Make a difference in the pharmaceutical industry from the comfort of your home.
- Qualifications: Experience in medical writing and knowledge of ICH guidelines required.
The predicted salary is between 40000 - 50000 £ per year.
Career Choices Dewis Gyrfa Ltd is looking for an experienced Medical Writer to support a leading Regulatory Affairs consultancy.
This role involves authoring, reviewing, and editing regulatory documents, collaborating with cross-functional teams.
The ideal candidate should have several years of medical writing experience in the pharmaceutical or biotech sectors, with a strong grasp of ICH guidelines and modules 2.5 and 2.7.
This fully remote opportunity is suited for UK-based professionals.
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Contact Details:
Career Choices Dewis Gyrfa Ltd Recruitment Team
We think you need these skills to ace Remote Regulatory Medical Writer – CTD Specialist (UK) in London
Medical Writing
Regulatory Document Authoring
ICH Guidelines Knowledge
Editing Skills
Collaboration with Cross-Functional Teams
Pharmaceutical Sector Experience
Biotech Sector Experience
