Regulatory Affairs Associate I
Mindlance
Job Title
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 Statement
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans
Vacancy posted 1 day ago
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