Remote Regulatory Publishing Specialist — Biotech

ProKidney is seeking a Regulatory Publishing Specialist to prepare submission-ready documents and manage QC on Word and PDF files. You will apply advanced editorial tools and coordinate with Regulatory Affairs, Medical Writing, and Quality teams to meet tight timelines.

The ideal candidate has 3–5 years in biotech or CRO settings, proficiency with PerfectIt, ISI Toolbox, ESG, Adobe Acrobat Pro, EndNote and SharePoint, and can work independently in a remote environment.