Scientific Writer (Regulatory Affairs Associate I)

100% ONSITE IRVINE CAPAY: $35-$38/hrMUST BE A LOCAL CANDIDATE. NO RELOCATIONREQUIRED:Bachelor's + 3–8 years or Master's + 2–6 years with Scientific writing (scientific reports, study reports, publications, or submissions)Ability to:Read, interpret, and summarize scientific dataProduce clean, structured, well-formatted documentsStrong attention to detail (formatting, tables, figures, footnotes)Background in:Biology, Chemistry, Bioengineering, or relatedExperience creating:Graphs / figures (Excel, Prism, etc.)Familiarity with document systems (Veeva/One Vault, SharePoint)Job Description:Supports early discovery / non-clinical work (no human clinical trials).Blend of:Scientific writingRegulatory-style documentation (light)High-volume report support and formattingCore ResponsibilitiesDraft, edit, and polish:Scientific reports (preclinical / early discovery)Regulatory-style documents (nonclinical modules)Abstracts, posters, and manuscripts (supporting role)Ensure documents are:Properly formatted (tables, figures, footnotes)Clear, consistent, and submission/presentation-readyGenerate and refine:Graphs, tables, and figures for reports and publicationsManage documentation systems:One Vault, SharePoint, ARCH/COSMOSSupport multiple concurrent projects (30+ active reports)Volume & Work Environment~2–3 regulatory-style submissions during contractHigh-volume environment with 30+ reports in progressFast-paced, deadline-driven:Frequent email communicationCross-functional coordinationShifting priorities, no fixed daily structure