Director of Regulatory Affairs and Content Strategy
18 hours ago
Job Summary
The Director of Regulatory Affairs and Content Strategy will provide senior level expertise and management for our client's medical writing team at Warman O'Brien.
This is a hybrid role in Central London, requiring the successful candidate to work on-site 4 days per week. The ideal candidate will have significant experience authoring pharmaceutical regulatory documentation across phases I-III.
Responsibilities
- Take full accountability for all medical writing and regulatory activities, ensuring optimal allocation of resources.
- Direct line management responsibilities for the Medical Writing team, with a focus on strategic leadership.
- Provide regulatory expertise to project teams on all aspects of the clinical trials process, supporting the organisation and preparation of regulatory submissions.
- Oversee the preparation and submission of all clinical study documentation in accordance with regulatory requirements.
- Establish and maintain excellent sponsor relationships, leveraging expertise to drive business growth.
Salary Information
We offer a competitive salary range of £80,000 - £120,000 per annum, commensurate with experience.
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