RCI-ABBV-33217 Scientific/Regulatory Writer (Publications/Journal/manuscript/Abs

Title: Scientific writer Onsite - Irvine, CA Contributions will include: generate graphs and figures for journal publications and poster presentations; Manage secure documentation systems such as One Vault, SharePoint, and ARCH/COSMOS; successful preparation of high-quality submission and presentation-ready documents; Ensure project information in publication records and resourcing tools are accurate and up-to-date. Responsibilities: Oversee controlled documents and processes: internal study reports and nonclinical modules of regulatory submissions. Oversee non-controlled documents: preparation of publication projects, journal manuscripts, abstracts, and posters. Manage documentation systems Complete miscellaneous scientific writing projects as needed. Qualifications: Bachelor’s degree in life sciences, clinical lab science or equivalent. Masters preferred. 3+ years of regulatory writing experience. Exhibits flexibility and a commitment to scientific excellence. Posses strong interpersonal and communication skills, with the ability to productively communicate with disparate personnel and departments.