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.
Possess strong interpersonal and communication skills, with the ability to productively communicate with disparate personnel and departments.
EEO:- Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans