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