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 documentsor- An established Regulatory CMC professional with a significant focus on technical writing and submission management, handling complex, data‐heavy documentationEssential experience:Proven involvement in drug development, ideally Phase IIIFlexibility on dosage formAbility to work independently and deliver to tight timelinesContract details:6‐month contract (high likelihood of extension)Fully remote (UK / EU)Competitive day rateShortlisting date: 18th March - please contact Mark Bux-Ryan for further details.