Regeneron Pharmaceuticals, Inc is hiring: Editor in Armonk
Regeneron Pharmaceuticals, Inc - Armonk, NY, United States, 10504
Work at Regeneron Pharmaceuticals, Inc
Overview
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Overview
The Editor will support the Head of Medical Writing Editing and more senior Medical Writing Editors by performing a full QC check of clinical regulatory documents, to ensure that they meet company standards and Health Authority guidelines. The Editor will train on more in-depth editing techniques and required to perform editing duties on various document types. As the individual’s editing/QC skills, knowledge of the drug development process and knowledge of regulatory document content increase, their responsibilities will increase.
As an Editor, a typical day might look like:
Work independently to perform high-quality QC checks of MW documents (eg, Submission Modules, CSRs, IBs)
Edit ICFs and Protocol Amendments; as knowledge and abilities improves, edit Protocols and IBs
Train on document editing and formatting for Submission Modules and CSRs
Work with more senior MWE staff to review and updates process improvement projects
Compile, verify content, and format appendices for CSRs
Ensures adherence to internal standards and procedures
To be considered for this role, you must have the following qualifications:
Education
Bachelor’s Degree or editor of life science (ELS) certification
Experience
2 years of relevant industry experience.
Technical reading, writing and editing skills.
Organizational, interpersonal and communication skills.
Solid understanding of MS Word, Adobe Acrobat, PowerPoint.
Ability to work independently.
Salary Range (annually)
$70,700.00 - $115,100.00
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