Senior Technical Writer – CMC (Consultant)
An experienced CMC Technical Writer is required to support late-stage drug development programmes, working on complex submission documentation within a fast‑paced development environment.
What we’re looking for:
* A strong background transitioning from Scientist to CMC Technical Writer, with several years’ experience authoring high‑quality CMC submission documents
or
* An established Regulatory CMC professional with a significant focus on technical writing and submission management, handling complex, data‑heavy documentation
Essential experience:
* Proven involvement in drug development, ideally Phase III
* Flexibility on dosage form
* Ability to work independently and deliver to tight timelines
Contract details:
* 6‑month contract (high likelihood of extension)
* Fully remote (UK / EU)
* Competitive day rate
Shortlisting date: 18th March - please contact Mark Bux-Ryan for further details