Senior Regulatory Writing Leader (Associate Director / Director / VP)
Location: UK (Hybrid or Remote options available)
I am partnered with a growing, high-performing regulatory and medical communications organisation to appoint an experienced Regulatory Writing leader at the Associate Director, Director, or VP level.
This is a key leadership role combining hands-on regulatory writing, team leadership, and strategic client engagement, offering the opportunity to shape both project delivery and the development of a high-calibre writing team.
The Role
* Lead the delivery of high-quality regulatory documents (e.g. CSRs, protocols, IBs, CTDs, INDs/NDAs/MAAs)
* Act as a subject matter expert, advising clients on regulatory strategy and documentation
* Manage and mentor regulatory writers, supporting development and performance
* Take ownership of multiple complex projects, ensuring quality, timelines, and client satisfaction
* Build strong client relationships, acting as a trusted partner on key programmes
* Contribute to business development, including proposals and expanding client engagements
Your Background
* Extensive experience in regulatory writing within pharma, biotech, CRO, or medical communications
* Proven ability to lead projects and teams in a fast-paced environment
* Strong knowledge of global regulatory requirements and submission documents
* Experience in client-facing roles and stakeholder management
* Passion for coaching, mentoring, and developing others
* Commercial awareness and interest in contributing to business growth
Why Apply?
* Join a collaborative, quality-driven organisation with strong growth
* Opportunity to step into a high-impact leadership role
* Blend of strategic influence and hands-on expertise
* Flexible working with a supportive, people-focused culture
If you’re interested in learning more, please apply or get in touch for a confidential discussion.