Consultant (H / F)

Overview

We are looking for an experienced Regulatory / Medical Writer who is ready to step into a more consultative, client-facing role. While you’ll bring deep hands-on expertise in regulatory document authorship, this position is focused less on day-to-day writing and more on guiding clients, providing best-practice recommendations, and ensuring the strategic and compliant delivery of high-quality regulatory documents.

What you’ll do

• Act as a trusted advisor to clients on regulatory writing deliverables, offering guidance on structure, compliance, and best practices.
• Oversee and review a broad range of documents (e.G., CSRs, IBs, PLSs ) to ensure alignment with ICH / GxP / GPP standards.
• Partner closely with client teams, offering scientific and regulatory insight that adds value beyond document production.
• Mentor and collaborate with writing teams, leveraging your background to ensure accuracy, clarity, and regulatory compliance.
• Represent the writing function confidently in meetings, workshops, and client interactions.

What we’re looking for

Why join us?

This is a unique opportunity for a writer who wants to evolve into a strategic, consultative role. You’ll still leverage your writing background every day, but instead of focusing on drafting, you’ll guide clients, shape deliverables, and influence best practices in regulatory writing.

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