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Scientific Writer

Planet Pharma, Irvine, CA, United States


Irvine, CA 6 month contract Target PR: 34-35/hr

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.