Scientific Writer

Target PR Range: 25-35/hr

• Depending on experience
  
  

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.