Regulatory Affairs Lead
2 weeks ago
We are seeking a highly skilled Regulatory Affairs Lead to join our team at Warman O'Brien. This is an exceptional opportunity for a senior-level expert to lead our medical writing and regulatory activities, ensuring optimal resource allocation and driving business growth.
Key Responsibilities:- Accountable for all medical writing and regulatory tasks, providing strategic guidance to project teams on clinical trials.
- Direct management of the Medical Writing team, fostering collaboration and innovation.
- Maintain strong sponsor relationships, leveraging expertise to drive regulatory submissions and study documentation preparation.
Main Requirements:
- 5-10 years of experience in authoring pharmaceutical regulatory documents across phases I-III.
- Desired: line management experience, with a proven track record of successful team leadership.
Location: Central London (occasional on-site work required)
Estimated Salary: 95000 - 110000 per annum depending on experience.
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