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
Strong background as a medical / regulatory writer within pharmaceutical companies, CROs, or regulatory service providers.
Proven familiarity with regulatory guidelines (ICH, GxP, GPP) and regulated deliverables (CSRs, IBs, PLSs).
Excellent communication skills, with the ability to translate technical writing expertise into client-facing consulting.
A detail-oriented, organized professional who can balance writing quality with broader consulting impact.
Experience in scientific communications a plus, but regulatory writing expertise is essential.
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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