Scientific Writer

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.