Senior Editor

Sorry, this job was removed at 08:15 p.m. (CST) on Friday, Jun 06, 2025
Hiring Remotely in United States
Remote
83K-135K Annually
Biotech • Pharmaceutical
The Role

The Senior Editor independently reviews or supervises quality control (QC) or review of nonclinical regulatory submission documents for spelling, grammar, consistency, accuracy, and adherence to company standards and styles. Maintains list(s) of QC comments/style questions and their resolutions within the group to ensure consistency within and/or between documents from multiple functional areas. Runs periodic review of internal guidance documents and templates. Collaborates with writing staff across a broad range of therapeutic areas and drug modalities.

As a Senior Editor, a typical day may include:

  • Editorial support for one or more of the following areas: Module 1 (Investigator’s Brochures and Development Safety Update Reports), Module 2 (nonclinical overview and introduction and nonclinical summaries), Module 3 (quality documents), and Module 4 (nonclinical study reports)

  • Review assigned documents/deliverables for spelling/grammar, style, consistency, and verification against source documentation from multiple functional areas

  • Build and maintain QC checklists for use throughout the group

  • Ensure editing staff adheres to the established QC review process

  • Lead initiatives for editing process improvements and software implementation

  • Lead and/or assist in training junior editing staff

  • Communicate clearly and in a timely manner to a wide range of people

To be considered for this role, you must have:

  • Minimum of a BS degree in life sciences

  • Minimum of 4 years of experience editing, formatting, drafting, or reviewing regulatory submission documents

  • Excellent interpersonal and communication (verbal and written) skills

  • Proficient in use of all software required for document drafting as well as document management platforms (eg, SharePoint and Veeva Vault RIM)

  • Sophisticated verbal and graphical data presentation skills

  • Strong understanding of the eCTD and the drug development process

  • Proven understanding of bioanalytical sciences and nonclinical subject matter supporting drug development (ie, pharmacokinetics, pharmacology, and toxicology) and ability to communicate this information with precision and transparency

  • Computer proficiency (Microsoft Office Suite [Word, Excel], Adobe Acrobat, EndNote, and related software) and proficiency in the English language is required

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.

Salary Range (annually)

$82,600.00 - $134,800.00

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The Company
HQ: New York, New York
15,000 Employees
Year Founded: 1988

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.

Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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