Scientific Writer
Planet Pharma, Irvine, CA, United States
Irvine, CA
6 month contract
Target PR: 34-35/hr
Check below to see if you have what is needed for this opportunity, and if so, make an application asap.
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. xywuqvp • Posses strong interpersonal and communication skills, with the ability to productively communicate with disparate personnel and departments.
Check below to see if you have what is needed for this opportunity, and if so, make an application asap.
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. xywuqvp • Posses strong interpersonal and communication skills, with the ability to productively communicate with disparate personnel and departments.