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For regulatory writers
Regulatory and medical writing roles, contract and permanent, including EU MDR and IVDR technical documentation, with clients who know the difference between a writer and a formatter.
Why people in your role call us
A job posting will ask for years of experience and a document type. It will not ask whether you can argue a benefit-risk position, hold a claim to what the data actually supports, or write a response that closes a review question rather than inviting three more.
So the screen selects for people who have produced documents, not people who have defended them. Then the client is surprised when the first draft needs rewriting by the medical director.
We screen for the argument. If you have taken a document through review questions and out the other side, that is what we put in front of the client.
Under 2 MB. PDF, DOC, DOCX, RTF, PPT or PPTX.
We never present your profile to a client without your permission. No fees, ever.
What we place you into
Modules, dossiers, briefing packages and responses to authority questions.
Protocols, clinical study reports and patient-facing summaries.
Technical documentation, clinical evaluation and post-market surveillance writing.
US device submissions, including predicate argumentation.
Manuscripts, abstracts and congress material.
Rewriting files that did not survive a gap assessment.
What we ask you
We ask about the argument, not the template.
If you can answer those properly you will be represented accurately, which is most of what goes wrong elsewhere.
Rates and timelines
Writing rates vary by document type, therapeutic complexity and whether the role is authoring or review. Device technical documentation and remediation work currently behave differently from traditional pharma writing.
We do not publish rate figures. What we do is tell you the client band before you interview, so you are not guessing what you are worth or discovering it at offer stage.
Typical time to first submission: Usually within a week; faster for device documentation, where demand is highest.
Questions
Related and not interchangeable, and clients are specific about which they want. We will tell you which of your experience is being sold.
Yes, and device documentation is currently where we see most demand, driven by EU MDR and IVDR remediation.
Mostly. Writing is one of the more genuinely remote disciplines we place.
Sometimes, particularly in device and remediation work. We will be candid about which clients will consider it rather than submitting you everywhere.
Both. Remediation and submission surges are contract; ongoing programme writing is often permanent.
Related
One conversation and you will know whether we can help.