Acadustri | Medical Writing jobs and careers

About Acadustri | Medical Writing

Your Science. Our Expertise. Clear, Compliant Medical Writing. Acadustri delivers expert clinical, regulatory, and safety medical writing for biotechnology and pharmaceutical companies. We turn complex data into clear, submission-ready documents that stand up to regulatory scrutiny. Supporting programmes from early development through to marketing authorisation and beyond, we work as an extension of your team to ensure your documentation is scientifically robust, consistent, and aligned with FDA, EMA, and MHRA expectations. What we do: > Clinical and regulatory writing: CSRs, IBs, protocols, informed consent, IND/NDA, IMPDs, orphan drug applications, briefing books and regulatory responses. > Pharmacovigilance and safety writing: DSURs, safety narratives, integrated summaries, RMPs/REMS, PSURs/PBRERs, post-marketing reports, benefit–risk assessments. > Publications and scientific communications: Manuscripts, literature reviews, congress materials, meeting reports, advisory boards, slide decks. > Acadustri InHouse: Your embedded medical writing team—providing scalable, audit-ready support, SOPs, templates, and strategic input across your organisation. Where we operate: United Kingdom, European Union, United States. If you are preparing for submission, responding to regulators, or scaling your medical writing capability, we can support you. Get in touch to discuss your requirements.