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 year of relevant industry experience.
Technical reading, writing and editing skills.
Organizational, interpersonal and communication skills.
Solid understanding of MS Word, Adobe Acrobat, PowerPoint.
Be able to work independently.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
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What We Do
At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.
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