Job Title: Senior Regulatory Medical Writer
Location: London, UK
Rate/Salary: 30000.00 - 75000.00 GBP Yearly
Job Type: Permanent
Responsibilities:
1. At least 3 years of relevant experience in writing study-related and submission-related clinical and regulatory documents.
2. Prepare a variety of clinical regulatory documents as the lead writer in collaboration with members of client authoring teams and supported by other writers, as appropriate.
3. Experience in writing Common Technical Document (CTD) modules, such as m2.5 Clinical Overview and m2.7s CTD summaries, and responding to Health Authority queries.
4. Leadership in delivering individual documents, setting clear expectations for timelines and quality.
5. Be responsible for providing document-specific advice to clients.
6. Project manage the timelines and review cycles of your documents.
7. Work in the client’s regulatory document management systems.
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